Schinzel A, Braegger C P, Brecevic L, Dutly F, Binkert F
Institute of Medical Genetics, University of Zürich, Switzerland.
J Med Genet. 1997 Aug;34(8):692-5. doi: 10.1136/jmg.34.8.692.
A very short, microcephalic, and mentally retarded 2 year old girl showed minor anomalies including prominent occiput, delayed closure of the anterior fontanelle, high frontal hairline, prominent ears, upward slanting palpebral fissures, a small nose with bulbous tip, delayed tooth eruption and bone maturation, and short and tapering fingers and toes. She did not have a white forelock. Cytogenetic investigation disclosed a de novo unbalanced translocation between chromosomes 4 and 18 with deletion of 4q12-->q21.1. Molecular investigation showed lack of a paternal allele for the microsatellite markers D4S392 and D4S398. This case shows indirect evidence that the piebald gene maps to proximal 4q12.
一名2岁的小头畸形且智力发育迟缓的女童,身材非常矮小,存在一些轻微异常,包括枕部突出、前囟闭合延迟、额部发际线高、耳朵突出、睑裂向上倾斜、鼻尖呈球状的小鼻子、出牙和骨骼成熟延迟,以及手指和脚趾短且呈锥形。她没有白色额发。细胞遗传学检查发现4号和18号染色体之间发生了新发的不平衡易位,4q12→q21.1缺失。分子检查显示微卫星标记D4S392和D4S398缺乏父本等位基因。该病例提供了间接证据,表明花斑病基因定位于4q12近端。