Autosomal recessive blepharophimosis, ptosis, V‐esotropia, syndactyly and short stature

M. Frydman*, H. A. Cohen, G. Karmon, H. Savir

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Frydman M, Cohen HA, Karmon G, Savir H. Autosomal recessive blepharophimosis, ptosis, V‐esotropia, syndactyly and short stature. Clin Genet 1992:41:57–61. 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 bead 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.

Original languageEnglish
Pages (from-to)57-61
Number of pages5
JournalClinical Genetics
Volume41
Issue number2
DOIs
StatePublished - Feb 1992

Keywords

  • autosomal recessive inheritance
  • blepharophimosis
  • eyelid disease
  • ptosis
  • short stature
  • strabismus
  • syndactyly

Fingerprint

Dive into the research topics of 'Autosomal recessive blepharophimosis, ptosis, V‐esotropia, syndactyly and short stature'. Together they form a unique fingerprint.

Cite this