Post-natal short stature, short limbs, brachydactyly, facial abnormalities, and delayed bone age:: A new syndrome?

被引:1
|
作者
Mégarbané, A
Rassi, S
Estephan, F
Kouba-Hreich, E
机构
[1] Univ St Joseph, Fac Med, Unite Genet Med, Beirut, Lebanon
[2] Hotel Dieu France Beyrouth, Serv ORL, Beirut, Lebanon
[3] Hotel Dieu France Beyrouth, Dermatol Serv, Beirut, Lebanon
[4] Ctr Med Psycho Pedag, Beirut, Lebanon
来源
AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2004年 / 125A卷 / 01期
关键词
brachydactyly; short stature; speech delay; delayed bone age; epicanthus;
D O I
10.1002/ajmg.a.20433
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A boy is described with clinical features including post-natal short stature, short limbs, speech delay, relatively large skull, prominent metopic ridge, wide palpebral fissures, proptosis, epicanthic folds, capillary hemangioma between the eyes and nose, flat nasal bridge, everted and small nares, small ears with a narrow external auditory canal and thick lobes, short neck, brachydactyly, bilateral Simian creases, a single flexion crease of the first and fifth fingers, protruding abdomen, and bilateral cryptorchidism. Radiographs did not show any features of bone dysplasia. However, a delayed bone age was noted. The boy's parents are first cousins. To the best of our knowledge, this constellation of anomalies has not been reported before, and may be considered a new syndrome. (C) 2003 Wiley-Liss, Inc.
引用
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页码:57 / 60
页数:4
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