Brothers with Chudley-McCullough Syndrome: Sensorineural Deafness, Agenesis of the Corpus Callosum, and other Structural Brain Abnormalities

American Journal of Medical Genetics

Volumn 124 A, Issue 1, 2004, Pages 74-78

  Østergaard, Elsebet ^a   Pedersen, Vibeke Faurholt ^b   Skriver, Elisabeth B ^b   Brøndum Nielsen, Karen ^a  

^a JOHN F KENNEDY INSTITUTE   (Denmark)

^b GLOSTRUP UNIVERSITY HOSPITAL   (Denmark)

Author keywords

Autosomal recessive; Chudley McCullough syndrome; Colpocephaly; Corpus callosum agenesis; Interhemispheric cyst; Sensorineural deafness; Structural brain abnormalities

Indexed keywords

ADOLESCENT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BRAIN CYST; BRAIN MALFORMATION; CASE REPORT; CHUDLEY MCCULLOUGH SYNDROME; CONSANGUINEOUS MARRIAGE; CORPUS CALLOSUM AGENESIS; GRAY MATTER; HEMISPHERE; HUMAN; HYDROCEPHALUS; MALE; PAKISTAN; PERCEPTION DEAFNESS; PRESCHOOL CHILD; PRIORITY JOURNAL;

GENETTA;

EID: 0942276987     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20380     Document Type: Article

References (6)

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3. Hendriks YMC, Laan LAEM, Vielvoye GJ, van Haeringen A. 1999. Bilateral sensorineural deafness, partial agenesis of the corpus callosum, and arachnoid cysts in two sisters. Am J Med Genet 86:183-186.
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5. Lemire EG, Stoeber GP. 2000. Chudley-McCullough syndrome: Bilateral sensorineural deafness, hydrocephalus, and other structural brain abnormalities. Am J Med Genet 90:127-130.
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