Abstract
Two sisters born to consanguineous Lebanese parents had mental retardation and epilepsy, brachymetacarpalia, hirsutism, bulbous soft nose, thick floppy ears with abnormal configuration and gingival hypertrophy. One girl presented additionally with tetralogy of Fallot and the other with congenital hypothyroidism and bilateral ureteral stenosis. These manifestations resemble the syndrome of hypertrichosis-gingival fibromatosis-mental retardation and seizures of Anavi et al. [1989: Dev Med Child Neurol 31:538-542] but our two girls additionally have brachymetacarpia. The inheritance seems to be autosomal recessive. These two sisters may represent a hitherto undescribed syndrome. We discuss the findings in our patients in relation to the literature. (C) 2000 Wiley-Liss, Inc.
| Original language | English |
|---|---|
| Journal | American Journal of Medical Genetics |
| Volume | 95 |
| Issue number | 3 |
| Pages (from-to) | 241-246 |
| Number of pages | 6 |
| ISSN | 0148-7299 |
| DOIs | |
| Publication status | Published - 27.11.2000 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Research Areas and Centers
- Research Area: Medical Genetics
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