Prenatal diagnosis of Chudley-McCullough syndrome
Author:
Affiliation:
1. Department of Radiology; Seattle Children's Hospital; University of Washington; Seattle Washington
2. Department of Pediatrics; Seattle Children's Hospital; University of Washington; Seattle Washington
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference14 articles.
1. GPSM2 and Chudley-McCullough syndrome: A Dutch founder variant brought to North America;Almomani;Am J Med Genet Part A,2013
2. Chudley-McCullough syndrome: Another report and a brief review of the literature;Alrashdi;Clin Dysmorphol,2011
3. Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: A newly described autosomal recessive disorder;Chudley;Am J Med Genet,1997
4. GPSM2 mutations in Chudley-McCullough syndrome;Diaz-Horta;Am J Med Genet Part A,2012
5. GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome;Doherty;Am J Hum Genet,2012
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1. Prenatal dispositions and genetic analysis of monozygotic female twins with suprasellar cysts and hydrocephalus: A case report;Child's Nervous System;2023-12-06
2. Cochlear implantation in a 16-month-old with Chudley-McCullough Syndrome;American Journal of Otolaryngology;2022-07
3. Chudley-McCullough syndrome;Radiopaedia.org;2022-06-24
4. Chudley–McCullough Syndrome: Case Report and the Role of Neuroimaging to Suggest the Diagnosis;Journal of Pediatric Neurology;2021-07-08
5. Fetal MRI assessment of posterior fossa anomalies: A review;Journal of Neuroimaging;2021-05-08
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