Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: specific entity or variant of a described condition?

American Journal of Medical Genetics Pub Date : 2000-11-27
G Göhlich-Ratmann, A Lackner, J Schaper, T Voit, G Gillessen-Kaesbach
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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.

两姐妹的牙龈肥大、多毛、智力迟钝和手掌短促综合征:特定的实体还是所描述疾病的变体?
黎巴嫩近亲父母所生的两个姐妹患有智力低下和癫痫、掌心短视、多毛症、球根状软鼻子、畸形的厚塌耳朵和牙龈肥大。一名女孩另外表现为法洛四联症,另一名患有先天性甲状腺功能减退和双侧输尿管狭窄。这些表现类似于Anavi等人的多毛综合征-牙龈纤维瘤病-智力迟钝和癫痫发作[1989:Dev Med Child Neurol 31:538-542],但我们的两个女孩还有掌心短促。遗传似乎是常染色体隐性遗传。这两姐妹可能代表一种迄今未被描述的综合症。我们根据文献讨论患者的发现。
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