Chudley–Mccullough syndrome

(Redirected from Chudley-Mccullough syndrome)

Chudley–Mccullough syndrome is a rare genetic disorder which is characterized by bilateral congenital (sometimes progressive) hearing loss associated with brain malformations.[1] It is a type of syndromic deafness.

Chudley–Mccullough syndrome
SpecialtyMedical genetics
SymptomsStructural brain abnormalities and hearing loss
ComplicationsHearing impairment
Usual onsetBirth
DurationLife-long
CausesGenetic mutation
Risk factorsBeing of Mennonite descent or being part of a consanguineous family (or both)
Diagnostic methodPhysical examination, MRIs, and genetic testing/whole genome sequencing/exome
Preventionnone
TreatmentTherapy
PrognosisGood
FrequencyVery rare. Approximately 20-30 cases have been reported in medical literature.

Presentation

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People with this disorder usually show the following symptoms:[2]

In some people with the disorder, arachnoid cysts, facial dysmorphisms, seizures and psycho-motor developmental delays (specific development spectrum disorders and intellectual disabilities) is found.[3]

Etimology

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This condition is associated with the GPSM2 gene.[4]

Cases

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What follows is a list of all cases of Chudley–Mccullough syndrome recorded in medical literature.[5]

  • 1997: Chudley et al. discovers the disorder by publishing the first case of the syndrome; they describe a brother and a sister born to second-cousin Canadian-Mennonite parents, both of the siblings showed hydrocephalus (caused by obstruction of the foramen of Monro and severe bilateral hearing loss. This case is then thought to be a brand new (novel) syndrome which is inherited in an autosomal recessive manner (due to both biological sexes being affected, absence of any intrauterine infections and the consanguineous parents being apparently healthy).[6]
  • 1999: Hendriks et al. describes two sisters with arachnoid cysts, congenital hearing loss, partial corpus callosum agenesis, and hydrocephalus. Though their parents were not close relatives, they came from the same small isolated village.[7]
  • 2000: ELemire et al. describes two Mennonite sisters with the disorder. The younger sister had congenital bilateral hearing loss and hydrocephalus due to obstruction of the foramen of Munro. She was found to have mutations in the FMR1 gene. The older sister had gray matter heterotopia, cortical dysplasia, dysgenesis of the corpus callosum and cerebellum, and congenital bilateral hearing loss.[8]
  • 2003: Oelrich Welch et al. describes three siblings (two brothers and one sister) with hearing loss, hydrocephalus, asymmetric dilatation of the lateral ventricles, arachnoid cysts, corpus callosum partial agenesis, and cerebellar cell migration anomalies.[9]
  • 2004: Østergaard et al. describes two siblings (more specifically, brothers) born to seemingly healthy, consanguineous Pakistani parents, both siblings had severe bilateral hearing loss and corpus callosum agenesis associated with other brain structure abnormalities.[10]
  • 2006: Matteucci et al. describes two Italian sisters born to non-consanguineous healthy parents. Both had hydrocephalus-induced macrocephaly, hearing loss, brain structure abnormalities, developmental delays, and minor facial dysmorphia.[11]
  • 2010: Shahin et al. and Walsh et al. described seven affected members from a large consanguineous Palestinian family. Those individuals had severe congenital hearing loss.[12][13]
  • 2011: Alrashdi et al. describes a 9-year-old girl born to consanguineous Lebanese parents, with infancy-onset hearing loss, hypoplasia of the inferior cerebellar vermis and corpus callosum, frontal parasagittal polymicrogyria, subcortical gray matter heterotopia, and cisterna magna enlargement. There was no foramen obstruction or abnormal psychomotor development.[14]
  • 2012: Yariz et al. describes a consanguineous Turkish family in which 3 members (all children) presented with congenital bilateral hearing loss and no other abnormalities; the 3 children had mutations in the GPSM2 gene.[15]
  • 2012: Doherty et al. describes 12 affected members from 8 families (including the first reported family with the disorder) with Chudley–McCullough syndrome, five out of the eight families were of Mennonite descent. All of the patients had severe bilateral hearing loss and brain structure anomalies. Two of the patients had manageable seizures and one had an intellectual disability of mild to moderate severity.[16]

References

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  1. ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Chudley McCullough syndrome". www.orpha.net. Retrieved 2022-05-19.{{cite web}}: CS1 maint: numeric names: authors list (link)
  2. ^ "Chudley-Mccullough syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2022-05-19.
  3. ^ "Chudley-McCullough syndrome (CMS) - UW Hindbrain Malformation Research Program". depts.washington.edu. Retrieved 2022-05-19.
  4. ^ Doherty, Dan; Chudley, Albert E.; Coghlan, Gail; Ishak, Gisele E.; Innes, A. Micheil; Lemire, Edmond G.; Rogers, R. Curtis; Mhanni, Aizeddin A.; Phelps, Ian G.; Jones, Steven J. M.; Zhan, Shing H. (2012-06-08). "GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome". The American Journal of Human Genetics. 90 (6): 1088–1093. doi:10.1016/j.ajhg.2012.04.008. ISSN 0002-9297. PMC 3370271. PMID 22578326.
  5. ^ "OMIM Entry - # 604213 - CHUDLEY-MCCULLOUGH SYNDROME; CMCS". omim.org. Retrieved 2022-05-19.
  6. ^ Chudley, A. E.; McCullough, C.; McCullough, D. W. (1997-01-31). "Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: a newly described autosomal recessive disorder". American Journal of Medical Genetics. 68 (3): 350–356. doi:10.1002/(sici)1096-8628(19970131)68:3<350::aid-ajmg19>3.0.co;2-s. ISSN 0148-7299. PMID 9024571.
  7. ^ Hendriks, Y. M.; Laan, L. A.; Vielvoye, G. J.; van Haeringen, A. (1999-09-10). "Bilateral sensorineural deafness, partial agenesis of the corpus callosum, and arachnoid cysts in two sisters". American Journal of Medical Genetics. 86 (2): 183–186. doi:10.1002/(SICI)1096-8628(19990910)86:2<183::AID-AJMG19>3.0.CO;2-U. ISSN 0148-7299. PMID 10449658.
  8. ^ Lemire, E. G.; Stoeber, G. P. (2000-01-17). "Chudley-McCullough syndrome: bilateral sensorineural deafness, hydrocephalus, and other structural brain abnormalities". American Journal of Medical Genetics. 90 (2): 127–130. doi:10.1002/(sici)1096-8628(20000117)90:2<127::aid-ajmg8>3.0.co;2-e. ISSN 0148-7299. PMID 10607951.
  9. ^ Welch, Katherine Oelrich; Tekin, Mustafa; Nance, Walter E.; Blanton, Susan H.; Arnos, Kathleen S.; Pandya, Arti (2003-05-15). "Chudley-McCullough syndrome: expanded phenotype and review of the literature". American Journal of Medical Genetics. Part A. 119A (1): 71–76. doi:10.1002/ajmg.a.10180. ISSN 1552-4825. PMID 12707963. S2CID 26098970.
  10. ^ Østergaard, Elsebet; Pedersen, Vibeke Faurholt; Skriver, Elisabeth B.; Brøndum-Nielsen, Karen (2004-01-01). "Brothers with Chudley-McCullough syndrome: sensorineural deafness, agenesis of the corpus callosum, and other structural brain abnormalities". American Journal of Medical Genetics. Part A. 124A (1): 74–78. doi:10.1002/ajmg.a.20380. ISSN 1552-4825. PMID 14679590. S2CID 45899320.
  11. ^ Matteucci, Fabio; Tarantino, Enrico; Bianchi, Maria Cristina; Cingolani, Cristina; Fattori, Bruno; Nacci, Andrea; Ursino, Francesco (2006-06-01). "Sensorineural deafness, hydrocephalus and structural brain abnormalities in two sisters: the Chudley-McCullough syndrome". American Journal of Medical Genetics. Part A. 140 (11): 1183–1188. doi:10.1002/ajmg.a.31178. ISSN 1552-4825. PMID 16642503. S2CID 35632735.
  12. ^ Walsh, Tom; Shahin, Hashem; Elkan-Miller, Tal; Lee, Ming K.; Thornton, Anne M.; Roeb, Wendy; Abu Rayyan, Amal; Loulus, Suheir; Avraham, Karen B.; King, Mary-Claire; Kanaan, Moien (2010-07-09). "Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82". American Journal of Human Genetics. 87 (1): 90–94. doi:10.1016/j.ajhg.2010.05.010. ISSN 1537-6605. PMC 2896776. PMID 20602914.
  13. ^ Shahin, Hashem; Walsh, Tom; Rayyan, Amal Abu; Lee, Ming K.; Higgins, Jake; Dickel, Diane; Lewis, Kristen; Thompson, James; Baker, Carl; Nord, Alex S.; Stray, Sunday (April 2010). "Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families". European Journal of Human Genetics. 18 (4): 407–413. doi:10.1038/ejhg.2009.190. ISSN 1476-5438. PMC 2987250. PMID 19888295.
  14. ^ Alrashdi, Ismail; Barker, Robert; Patton, Michael A. (April 2011). "Chudley-McCullough syndrome: another report and a brief review of the literature". Clinical Dysmorphology. 20 (2): 107–110. doi:10.1097/MCD.0b013e328341d007. ISSN 1473-5717. PMID 21127420.
  15. ^ Yariz, K. O.; Walsh, T.; Akay, H.; Duman, D.; Akkaynak, A. C.; King, M.-C.; Tekin, M. (March 2012). "A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss". Clinical Genetics. 81 (3): 289–293. doi:10.1111/j.1399-0004.2011.01654.x. ISSN 1399-0004. PMC 3657750. PMID 21348867.
  16. ^ Doherty, Dan; Chudley, Albert E.; Coghlan, Gail; Ishak, Gisele E.; Innes, A. Micheil; Lemire, Edmond G.; Rogers, R. Curtis; Mhanni, Aizeddin A.; Phelps, Ian G.; Jones, Steven J. M.; Zhan, Shing H. (2012-06-08). "GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome". American Journal of Human Genetics. 90 (6): 1088–1093. doi:10.1016/j.ajhg.2012.04.008. ISSN 1537-6605. PMC 3370271. PMID 22578326.