Blepharophimosis: a causally heterogeneous malformation frequently associated with developmental disabilities.

Abstract

We report on 22 individuals referred for genetic evaluation because of blepharophimosis. Fourteen of these patients had the blepharophimosis syndrome: 5 familial and 9 sporadic. Mental retardation or developmental delay was seen in 8 of the 12 children in whom this could be assessed. Eight of 22 children had a malformation syndrome other than the blepharophimosis syndrome. All 8 of these children were mentally retarded or developmentally delayed. Two of these 8 had recognized disorders (branchio-oto-renal syndrome and a ring 4 chromosome); the remaining 6 had unrecognized malformation syndromes. Based on this information, it is suggested that children with blepharophimosis be evaluated carefully for underlying conditions and that they be observed for developmental disabilities because of the frequent association.

• Authors: C Cunniff, M Curtis, S J Hassed, H E Hoyme
• Journal: American journal of medical genetics (Am J Med Genet) Vol. 75 Issue 1 Pg. 52-4 (Jan 06 1998) ISSN: 0148-7299 [Print] United States
• PMID: 9450857 (Publication Type: Journal Article)

Topics

• Blepharophimosis (genetics)
• Child
• Chromosomes, Human, Pair 3
• Developmental Disabilities (genetics)
• Female
• Genes, Dominant (genetics)
• Humans
• Intellectual Disability (genetics)
• Male
• Syndrome