Literature DB >> 1311991

Autosomal recessive blepharophimosis, ptosis, V-esotropia, syndactyly and short stature.

M Frydman1, H A Cohen, G Karmon, H Savir.   

Abstract

A recessively inherited syndrome of blepharophimosis and ptosis with weakness of extraocular and frontal muscles is reported in six members of three related kindreds. Prognathism, synophrys and thick eyebrows added to a typical facial appearance. Additional findings included short stature, borderline head circumference and toe syndactyly. Borderline mental retardation and anosmia were found in one patient. The clinical features and the mode of inheritance distinguish this syndrome from other blepharophimosis and ptosis syndromes.

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Year:  1992        PMID: 1311991     DOI: 10.1111/j.1399-0004.1992.tb03632.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  1 in total

1.  Frydman-Cohen-Karmon syndrome: a rare syndromic association of blepharophimosis.

Authors:  Rachna Meel; Nikitha Ayyadurai; Sahil Agrawal; Deepsekhar Das
Journal:  BMJ Case Rep       Date:  2020-06-29
  1 in total

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