Hypertrichosis, hyperkeratosis, abnormal corpus callosum, mental retardation and dysmorphic features in three unrelated females
- 1 April 2004
- journal article
- case report
- Published by Wolters Kluwer Health in Clinical Dysmorphology
- Vol. 13 (2) , 85-90
- https://doi.org/10.1097/00019605-200404000-00006
Abstract
We report three unrelated patients with hypertrichosis, mild to moderate mental retardation, and dysmorphic facial features including low anterior hairline, thick arched eyebrows, nose with broad tip and columella below alae nasi, short philtrum, thick drooping lower lip and simple posteriorly rotated ears. They also had rough skin with hyperkeratotic plaques. Feet and finger tips were broad. All of them had personality problems like aggressiveness, stubborn temperament or tendency to withdraw. Brain MRI showed thick and short corpus callosum. We believe that these patients represent a new syndrome of unknown aetiology.Keywords
This publication has 9 references indexed in Scilit:
- Zimmermann–Laband syndrome associated with a balanced reciprocal translocation t(3;8)(p21.2;q24.3) in mother and daughter: Molecular cytogenetic characterization of the breakpoint regionsAmerican Journal of Medical Genetics Part A, 2003
- Delineation of a newly recognized neurocutaneous malformation syndrome with “cutis tricolor”American Journal of Medical Genetics Part A, 2003
- Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBPJournal of Medical Genetics, 2002
- Inherited hypertrichosesClinical Genetics, 2002
- Hajdu-Cheney syndrome: Evolution of phenotype and clinical problemsAmerican Journal of Medical Genetics, 2001
- Growth deficiency, mental retardation and unusual faciesClinical Dysmorphology, 2000
- FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancyEuropean Journal of Human Genetics, 1999
- Three patients with the osteochondrodysplasia and hypertrichosis syndrome - Cantu syndromeClinical Dysmorphology, 1998
- Construction of a 1.2-Mb Contig Surrounding, and Molecular Analysis of, the Human CREB-Binding Protein (CBP/CREBBP) Gene on Chromosome 16p13.3Genomics, 1997