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A newly recognized skeletal dysplasia with rhizomelic limbs and retinitis pigmentosa
Author(s) -
Mégarbané André,
Melick Nancy,
Daou Linda
Publication year - 2004
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.30138
Subject(s) - retinitis pigmentosa , medicine , dysplasia , ophthalmology , anatomy , retinal
A girl with severe pre‐ and post‐natal short stature, low‐pitched voice, retinitis pigmentosa, photophobia, short neck, broad thorax, platyspondyly, rhizomelic shortening of the long bones, bilateral subluxation of the hips, advanced maturation of the epiphyses, and apparently normal intellectual development is described. The girl's parents are first cousins. Two subsequent pregnancies had ended in spontaneous abortion with polyhydramnios and severe growth retardation. To the best of our knowledge, this association had not been previously reported, and may be considered a newly recognized syndrome. © 2004 Wiley‐Liss, Inc.