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MP 2.04.81 Genetic Testing for Rett Syndrome

Medical Policy    
Original Policy Date
 July 2012
Last Review Status/Date
Reviewed with literature search/9:2014
  Return to Medical Policy Index


Our medical policies are designed for informational purposes only and are not an authorization, or an explanation of benefits, or a contract.  Receipt of benefits is subject to satisfaction of all terms and conditions of the coverage.  Medical technology is constantly changing, and we reserve the right to review and update our policies periodically. 


Rett syndrome (RTT) is a severe neurodevelopmental disorder primarily affecting girls with an incidence of 1:10,000 female births, making it one of the most common genetic causes of intellectual disability in girls. (2) RTT is characterized by apparent normal development for the first 6-18 months of life, followed by the loss of intellectual functioning, loss of acquired fine and gross motor skills and the ability to engage in social interaction. Purposeful use of the hands is replaced by repetitive stereotyped hand movements, sometimes described as hand-wringing. (1) Other clinical manifestations include seizures, disturbed breathing patterns with hyperventilation and periodic apnea, scoliosis, growth retardation and gait apraxia. (3)

There is wide variability in the rate of progression and severity of the disease. In addition to the classical form of RTT, there are a number of recognized atypical variants. Variants of RTT may appear with a severe or a milder form. The severe variant has no normal developmental period; individuals with a milder phenotype experience less dramatic regression and milder expression of the characteristics of classical RTT.

The diagnosis of RTT remains a clinical one, using diagnostic clinical criteria that have been established for the diagnosis of classic and variant Rett syndrome. (1-3)

Treatment of Rett syndrome

Currently, there are no specific treatments that halt or reverse the progression of the disease, and there are no known medical interventions that will change the outcome of patients with RTT. Management is mainly symptomatic and individualized, focusing on optimizing each patient’s abilities.(2) A multidisciplinary approach is usually applied, with specialist input from dietitians, physiotherapists, occupational therapists, speech therapists and music therapists. Regular monitoring for scoliosis (seen in 87% of patients by age 25 years) and possible heart abnormalities may be recommended. Spasticity can have a major impact on mobility; physical therapy and hydrotherapy may prolong mobility. Occupational therapy can help children develop communication strategies and skills needed for performing self-directed activities (eg, dressing, feeding, practicing arts and crafts).

Pharmacologic approaches to managing problems associated with RTT include melatonin for sleep disturbances and several agents for the control of breathing disturbances, seizures, and stereotypic movements. RTT patients have an increased risk of life-threatening arrhythmias associated with a prolonged QT interval, and avoidance of a number of drugs is recommended, including prokinetic agents, antipsychotics, tricyclic antidepressants, antiarrhythmics, anesthetic agents and certain antibiotics.

In a mouse model of RTT, genetic manipulation of mutated MECP2 has demonstrated reversibility of the genetic defect.(4,5)

Genetics of Rett syndrome

RTT is an X-linked dominant genetic disorder. Mutations in MECP2, which is thought to control expression of several genes including some involved in brain development, were first reported in 1999. Subsequent screening has shown that over 80% of patients with classical RTT have pathogenic mutations in the MECP2 gene. More than 200 mutations in MECP2 have been associated with RTT.(6) However, 8 of the most commonly occurring missense and nonsense mutations account for almost 70% of all cases; small C-terminal deletions account for approximately 10%; and large deletions, 8% to 10%.(7) MECP2 mutation type is associated with disease severity.(8) Whole duplications of the MECP2 gene have been associated with severe X-linked intellectual disability with progressive spasticity, no or poor speech acquisition, and acquired microcephaly. Additionally, the pattern of X-chromosome inactivation influences the severity of the clinical disease in females.(9,10)

Because the spectrum of clinical phenotypes is broad, to facilitate genotype-phenotype correlation analyses, the International Rett Syndrome Association has established a locus-specific MECP2 variation database (RettBASE) and a phenotype database (InterRett).

Approximately 99.5% of cases of RTT are sporadic, resulting from a de novo mutation, which arise almost exclusively on the paternally derived X chromosome. The remaining 0.5% of cases are familial and usually explained by germline mosaicism or favorably skewed X-chromosome inactivation in the carrier mother that results in her being unaffected or only slightly affected (mild intellectual disability). In the case of a carrier mother, the recurrence risk of RTT is 50%. If a mutation is not identified in leukocytes of the mother, the risk to a sibling of the proband is below 0.5% (because germline mosaicism in either parent cannot be excluded).

Identification of a mutation in MECP2 does not necessarily equate to a diagnosis of RTT. Rare cases of MECP2 mutations also have been reported in other clinical phenotypes, including individuals with an Angelman-like picture, nonsyndromic X-linked intellectual disability, PPM-X syndrome (an X-linked genetic disorder characterized by psychotic disorders [most commonly bipolar disorder], parkinsonism, and intellectual disability), autism, and neonatal encephalopathy.(2,6,11)

A proportion of patients with a clinical diagnosis of RTT do not appear to have mutations in the MECP2 gene. Two other genes, CDKL5 and FOXG1, have been shown to be associated with atypical variants.

Regulatory Status

No U.S. Food and Drug Administration (FDA)-cleared genotyping tests were found. Thus, genotyping is offered as a laboratory-developed test. Clinical laboratories may develop and validate tests in-house (“home-brew”) and market them as a laboratory service; such tests must meet the general regulatory standards of the Clinical Laboratory Improvement Act (CLIA). The laboratory offering the service must be licensed by CLIA for high-complexity testing.




Mutation testing for Rett syndrome may be considered medically necessary to confirm a diagnosis of Rett syndrome in a female child with developmental delay and signs/symptoms of Rett syndrome, but when there is uncertainty in the clinical diagnosis.

All other indications for mutation testing for Rett syndrome, including prenatal screening and testing of family members, are considered investigational.

Policy Guidelines 


Beginning in 2012, there is specific CPT coding for this testing:

81302: MECP2 (methyl CpG binding protein 2)(eg, Rett syndrome) gene analysis; full sequence analysis

81303: known familial variant

81304: duplication/deletion variants

CPT code 81404 includes the following testing for FOXG1:

FOXG1 (forkhead box G1)(eg, Rett syndrome), full gene sequence

CPT code 81406 includes the following testing for CDKL5:

CDKL5 (cyclin-dependent kinase-like 5)(eg., epileptic encephalopathy), full gene sequence

Benefit Application
BlueCard/National Account Issues 

No applicable information 


This policy was created in 2012 and is based on a search of the MEDLINE database through August 18, 2014. Literature that describes the analytic validity, clinical validity, and clinical utility of genetic testing for RTT was sought.

Analytic Validity
Analytic validity is the technical accuracy of the test in detecting a mutation that is present or in excluding a mutation that is absent) The test is generally done as full gene sequencing of the MECP2 gene to diagnose atypical or classic Rett syndrome (RTT) and as multiplex ligation probe amplification (MLPA) for duplication/deletion analysis. Familial mutation testing may be done with targeted sequencing. CDKL5  sequencing may be done for atypical RTT.

According to a large reference laboratory, MECP2 testing for RTT has an analytic sensitivity for sequencing of 99% and for MLPA, 90%; analytic specificity is 99% for sequencing and for MLPA, 98%.(12)

Clinical Validity
Clinical validity is the diagnostic performance of the test (sensitivity, specificity, and positive and negative predictive values) in detecting clinical disease.

Huppke et al (2000) analyzed the MECP2 gene in 31 female patients diagnosed clinically with RTT.(13) Sequencing revealed mutations in 24 of the 31 patients (77%). Of the 7 patients in whom no mutations were found, 5 fulfilled criteria for classical RTT. In this study, 17 different mutations were detected, 11 of which had not been previously described. Several females carrying the same mutation displayed different phenotypes, suggesting that factors other than the type or position of mutations influenced the severity of RTT.

Cheadle et al (2000) analyzed mutations in 48 females with classical sporadic RTT, 7 families with possible familial RTT, and 5 sporadic females with features suggestive, but not diagnostic, of RTT.(14) The entire MECP2 gene was sequenced in all cases. Mutations were identified in 44 (80%) of 55 unrelated classical sporadic and familial RTT patients. Only 1 (20%) of 5 sporadic cases with suggestive but nondiagnostic features of RTT had mutations identified. Twenty-one different mutations were identified (12 missense, 4 nonsense, and 5 frame-shift mutations); 14 of the mutations identified were novel. Significantly milder disease was noted in patients carrying missense mutations as compared with those with truncating mutations.

The 2 studies previously outlined were included in a summary of 6 articles by Lotan et al (2006) who attempted to disclose a genotype-phenotype correlation.(3) The authors found that these studies have yielded inconsistent results and that further controlled studies are needed before valid conclusions can be drawn about the effect of mutation type on phenotypic expression. Two subsequent studies(15,16) used he InterRett database to examine genotype and RTT severity. Of 357 girls with epilepsy who had MECP2 genotype recorded, those with large deletions were more likely than those with 10 other common mutations to have active epilepsy (odds ratio [OR], 3.71; 95% confidence interval [CI], 1.13 to 12.17; p=0.03) and had the earliest median age at epilepsy onset (3 years 5 months). Among all girls in the database, those with large deletions were more likely to have never walked (OR=0.42; 95% CI, 0.22 to 0.79; p=0.007). Of 260 girls with classic RTT enrolled in the multicenter RTT Natural History study (NCT00299312), those with the R133C substitution mutation had clinically less severe disease, assessed by the Clinical Severity, Motor Behavior Analysis, and Physician Summary scales.(7) Fabio et al (2014) reported similar genotype-phenotype correlations among 144 patients with RTT in Italy.(17)

Section Summary

Evidence from several small studies has indicated that the clinical sensitivity of genetic testing for classical RTT is reasonably high, in the range of 75% to 80%. However, sensitivity may be lower when classic RTT features are absent. Clinical specificity is unknown but also is likely to be high, as only rare cases of MECP2 mutations have been reported in other clinical phenotypes, including individuals with an Angelman-like picture, nonsyndromic X-linked intellectual disability, PPM-X syndrome, autism and neonatal encephalopathy.

Clinical Utility
Clinical utility is how results of the diagnostic test will be used to change management of the patient and whether these changes in management lead to clinically important improvements in health outcomes).

The clinical utility of genetic testing can be considered in the following clinical situations: (1) individuals with suspected RTT, (2) family members of individuals with RTT, and (3) prenatal testing for mothers with a previous RTT child. These situations will be discussed separately next.

Individuals With Suspected RTT

The clinical utility for these patients depends on the ability of genetic testing to make a definitive diagnosis and for that diagnosis to lead to management changes that improve outcomes. No studies were identified that described how a molecular diagnosis of RTT changed patient management. Therefore, there is no direct evidence for the clinical utility of genetic testing in these patients.

There is no specific treatment for RTT, so that making a definitive diagnosis will not lead to treatment that alters the natural history of the disorder. There are several potential ways in which adjunctive management might be changed after genetic confirmation of the diagnosis:

  • Further diagnostic testing may be avoided
  • Referral to a specialist(s) may be made
  • Heightened surveillance for Rett-associated clinical manifestations, such as scoliosis or cardiac arrhythmias may be performed
  • More appropriate tailoring of ancillary treatments such as occupational therapy may be possible

Family Members

Genetic testing can be done in sisters of girls with RTT who have an identified MECP2 mutation to determine if they are asymptomatic carriers of the disorder. However, this is an extremely rare possibility, because the disorder is nearly always sporadic. Testing of family members of individuals with RTT will therefore result in an extremely low yield.

Prenatal Screening

It may be appropriate to offer prenatal diagnosis to a couple who have had a child with RTT or intellectual disability due to a MECP2 mutation. Because the disorder occurs spontaneously in most affected individuals, however, the risk of a family having a second child with the disorder is less than 1%, except in the rare situation where the mother carries the mutation.(18) Therefore, for mothers without the Rett phenotype, it is extremely unlikely that prenatal testing will identify cases of RTT.

Section Summary

The clinical utility of genetic testing for RTT has not been established in the literature, however, genetic testing can confirm the diagnosis in patients with clinical signs and symptoms of RTT, and management changes may result. In addition, a definitive diagnosis can avoid further testing for other possible diagnoses. For testing family members and for prenatal testing, clinical utility is lacking, because the yield of testing in those situations is extremely low.

Ongoing and Unpublished Clinical Trials

The online site currently lists several active trials of treatments for RTT: desipramine (NCT00990691); dextromethorphan (NCT01520363); recombinant insulin-like growth factor-1 (NCT01777542); fingolimod (NCT02061137); glatiramer acetate (NCT02023424, NCT02153723); and allogeneic bone marrow transplantation for males with Rett syndrome (NCT02171104).

Clinical Input Received From Physician Specialty Societies and Academic Medical Centers

In response to requests, input related to the use mutation testing for Rett syndrome was received in June 2012 from 3 academic medical centers and 2 specialty medical societies (3 reviewers), for a total of 6 reviewers. While the various physician specialty societies and academic medical centers may collaborate with and make recommendations during this process, through the provision of appropriate reviewers, input received does not represent an endorsement or position statement by the physician specialty societies or academic medical centers, unless otherwise noted.

There was consensus/near total consensus supporting the use of mutation testing for the diagnosis of RTT in a girl in whom the clinical differential diagnosis includes RTT, especially when clinical diagnosis is uncertain. Support for testing sisters of individuals with RTT and for prenatal screening was mixed.

Summary of Evidence

MECP2 mutations are found in most patients with Rett syndrome (RTT), particularly those who present with classical clinical features of RTT. Diagnostic accuracy of mutation testing for RTT cannot be determined with absolute certainty given the lack of a true criterion standard for RTT diagnosis, but testing appears to have high sensitivity and specificity.

Testing for MECP2 mutations has clinical utility in certain clinical scenarios. The diagnosis of RTT is considered to be a clinical one, characterized by a specific developmental profile that should meet certain clinical diagnostic criteria.(1) Certain atypical variants of RTT may be more difficult to diagnose clinically, and MECP2 mutation testing may be useful in confirming or excluding the diagnosis of RTT. Although
there is no effective treatment for RTT, and management is mainly supportive, a definitive diagnosis can end a diagnostic workup for other possible diagnoses and may alter some aspects of management (eg, determining whether or not to advise avoidance of medications that can prolong QT interval).

Testing of family members and prenatal testing in a couple who have had a child with RTT or intellectual disability due to a MECP2 mutation is not likely to improve outcomes. The risk of a family having a second child with the disorder is less than 1%, except in the rare situation where the mother carries the mutation, and the impact on decision making on health outcomes is uncertain.

Therefore, mutation testing for RTT may be considered medically necessary to confirm a diagnosis of RTT in a female child with developmental delay and signs/symptoms of RTT when there is uncertainty in the clinical diagnosis. All other indications for mutation testing for RTT, including prenatal screening and testing of family members, are considered investigational.

Practice Guidelines and Position Statements
American Academy of Neurology/Child Neurology Society

In 2011, a quality standards subcommittee of American Academy of Neurology (AAN) and the Practice Committee of the Child Neurology Society issued an evidence report on the genetic and metabolic testing of children with global developmental delay.(19) AAN recommended considering MECP2 mutation testing for all girls with unexplained moderate to severe developmental delay.

American Academy of Pediatrics

A 2007 policy statement from the American Academy of Pediatrics (AAP; reaffirmed in 2010(20))recommended MECP2 testing to confirm a diagnosis of suspected RTT, especially when the diagnosis was unclear from symptoms alone.(21)


Neither AAN nor AAP have provided recommendations on when to use CDKL5 or FOXG1 testing. In 2010, RettSearch, a consortium of international clinical RTT specialists, suggested that patients who are negative for MECP2 mutations and who have a strong clinical diagnosis of RTT should be considered for further screening for the CDKL5 gene if there are early onset seizures, or for the FOXG1 gene if there are
congenital features (eg, severe postnatal microcephaly).(1) This suggestion is supported by other authors.(2)

American College of Medical Genetics

In 2013, the American College of Medical Genetics revised its evidence-based guideline for clinical genetics evaluation of autism spectrum disorders.(22) Testing for MECP2 mutations is recommended as part of the diagnostic workup of females who present with an autistic phenotype. Routine MECP2 testing in males with autistic spectrum disorders is not recommended.

U.S. Preventive Services Task Force Recommendations
Genetic testing for RTT is not a preventive service.

Medicare National Coverage
There is no national coverage determination (NCD). In the absence of an NCD, coverage decisions are left to the discretion of local Medicare carriers.


  1. Neul JL, Kaufmann WE, Glaze DG, et al. Rett syndrome: revised diagnostic criteria and nomenclature. Ann Neurol. Dec 2010;68(6):944-950. PMID 21154482
  2. Williamson SL, Christodoulou J. Rett syndrome: new clinical and molecular insights. Eur J Hum Genet. Aug 2006;14(8):896-903. PMID 16865103
  3. Lotan M, Ben-Zeev B. Rett syndrome. A review with emphasis on clinical characteristics and intervention. ScientificWorldJournal. 2006;6:1517-1541. PMID 17160339
  4. Guy J, Gan J, Selfridge J, et al. Reversal of neurological defects in a mouse model of Rett syndrome. Science. Feb 23 2007;315(5815):1143-1147. PMID 17289941
  5. Robinson L, Guy J, McKay L, et al. Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome. Brain. Sep 2012;135(Pt 9):2699-2710. PMID 22525157
  6. Suter B, Treadwell-Deering D, Zoghbi HY, et al. Brief report: MECP2 mutations in people without Rett syndrome. J Autism Dev Disord. Mar 2014;44(3):703-711. PMID 23921973
  7. Lane JB, Lee HS, Smith LW, et al. Clinical severity and quality of life in children and adolescents with Rett syndrome. Neurology. Nov 15 2011;77(20):1812-1818. PMID 22013176
  8. Cuddapah VA, Pillai RB, Shekar KV, et al. Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome. J Med Genet. Mar 2014;51(3):152-158. PMID 24399845
  9. Archer H, Evans J, Leonard H, et al. Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation. J Med Genet. Feb 2007;44(2):148-152. PMID 16905679
  10. Weaving LS, Williamson SL, Bennetts B, et al. Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotype. Am J Med Genet A. Apr 15 2003;118A(2):103-114. PMID 12655490
  11. Liyanage VR, Rastegar M. Rett syndrome and MeCP2. Neuromolecular Med. Jun 2014;16(2):231-264. PMID 24615633
  12. ARUP Laboratories. Rett Syndrome (MECP2): sequencing and deletion/duplication. Accessed August 2014.
  13. Huppke P, Laccone F, Kramer N, et al. Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients. Hum Mol Genet. May 22 2000;9(9):1369-1375. PMID 10814718
  14. Cheadle JP, Gill H, Fleming N, et al. Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location. Hum Mol Genet. Apr 12 2000;9(7):1119-1129. PMID 10767337
  15. Bao X, Downs J, Wong K, et al. Using a large international sample to investigate epilepsy in Rett syndrome. Dev Med Child Neurol. Jun 2013;55(6):553-558. PMID 23421866
  16. Bebbington A, Downs J, Percy A, et al. The phenotype associated with a large deletion on MECP2. Eur J Hum Genet. Sep 2012;20(9):921-927. PMID 22473088
  17. Fabio RA, Colombo B, Russo S, et al. Recent insights into genotype-phenotype relationships in patients with Rett syndrome using a fine grain scale. Res Dev Disabil. Aug 11 2014;35(11):2976-2986. PMID 25124696
  18. Amir RE, Sutton VR, Van den Veyver IB. Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy. J Child Neurol. Sep 2005;20(9):779-783. PMID 16225835
  19. Michelson DJ, Shevell MI, Sherr EH, et al. Evidence report: Genetic and metabolic testing on children with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology. Oct 25 2011;77(17):1629-1635. PMID 21956720
  20. AAP publications retired and reaffirmed. Pediatrics. Dec 2010;126:e1622. PMID
  21. Johnson CP, Myers SM. Identification and evaluation of children with autism spectrum disorders. Pediatrics. Nov 2007;120(5):1183-1215. PMID 17967920
  22. Schaefer GB, Mendelsohn NJ. Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions. Genet Med. May 2013;15(5):399-407. PMID 23519317




CPT  81302 MECP2 (methyl CpG binding protein 2)(eg, Rett syndrome) gene analysis; full sequence analysis
  81303 MECP2 (methyl CpG binding protein 2)(eg, Rett syndrome) gene analysis; known familial variant


MECP2 (methyl CpG binding protein 2)(eg, Rett syndrome) gene analysis; duplication/deletion variants
ICD-9-CM Diagnosis   Investigational for all diagnoses
ICD-10-CM (effective 10/1/15)   Investigational for all diagnoses
  F84.2 Rett's syndrome
  Z13.4 Encounter for screening for certain developmental disorders in childhood
ICD-10-PCS (effectve 10/1/15)    Not applicable. ICD-10-PCS codes are only used for inpatient services. There are no ICD procedure codes for laboratory tests.


Genetic Testing, Rett Syndrome
MECP2, Genetic Testing

Policy History


Date Action Reason
07/12/12 Add to Medicine -Pathology/Laboratory section New policy. Policy statements state that mutation testing for Rett syndrome may be considered medically necessary to confirm a diagnosis of Rett syndrome in a female child with developmental delay and signs/symptoms of Rett syndrome, but when there is uncertainty in the clinical diagnosis. All other indications for mutation testing for Rett syndrome, including prenatal screening and testing of family members, are considered investigational.
8/09/12 Replace policy- correction only Last paragraph of the Summary section revised for clarification and diagnosis codes added to code table.
9/12/13 Replace policy Policy updated with a literature search through July 2013; references 3-6, 10 and 11 added. Policy statements unchanged.
9/11/14 Replace policy Policy updated with literature review through August 18, 2014; references 6, 8-11, 17, and 19-22 added; reference 12 updated. No change to policy statements.


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