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

Gudrun Göhlich-Ratmann, Anja Lackner, J. Schaper, T. Voit, Gabriele Gillessen-Kaesbach*

*Corresponding author for this work

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 languageEnglish
JournalAmerican Journal of Medical Genetics
Volume95
Issue number3
Pages (from-to)241-246
Number of pages6
ISSN0148-7299
DOIs
Publication statusPublished - 27.11.2000

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Areas and Centers

  • Research Area: Medical Genetics

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