Chudley-McCullough syndrome
Publisher
Radiopaedia.org
Reference7 articles.
1. Matteucci F, Tarantino E, Bianchi M et al. Sensorineural Deafness, Hydrocephalus and Structural Brain Abnormalities in Two Sisters: The Chudley–McCullough Syndrome. Am J Med Genet. 2006;140A(11):1183-8.
2. Alrashdi I, Barker R, Patton M. Chudley–McCullough Syndrome: Another Report and a Brief... : Clinical Dysmorphology. LWW. 2011;20(2):107-10.
3. Blauen A, Stutterd C, Stouffs K et al. Chudley-McCullough Syndrome: A Recognizable Clinical Entity Characterized by Deafness and Typical Brain Malformations. J Child Neurol. 2020;36(2):152-8.
4. Chapman T, Perez F, Ishak G, Doherty D. Prenatal Diagnosis of Chudley-McCullough Syndrome. Am J Med Genet. 2016;170(9):2426-30.
5. Doherty D, Chudley A, Coghlan G et al. GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome. Am J Hum Genet. 2012;90(6):1088-93.