Prabhu V G, Kozma C, Leftridge C A, Helmbrecht G D, France M L
Department of Pediatrics, Georgetown University Medical Center, Washington, DC 20007-3935, USA.
Am J Med Genet. 1998 Jan 13;75(2):164-70.
We report on a male infant born with clinical and radiographic evidence of a lethal form of dyssegmental dysplasia not comparable to Silverman-Handmaker type, who had a prolonged survival of more than eight months. He had ocular and central nervous system abnormalities which have not been previously described. His course included significant feeding and respiratory difficulties, severe physical and psychomotor retardation, and recurrent fever of unknown etiology believed to be of central origin. The relatively long survival of this infant enabled us to focus on the natural history of this rare syndrome. The infant was born to first cousin parents of Druze Lebanese origin supporting an autosomal recessive mode of inheritance for the condition. This is the first documentation of dyssegmental dysplasia Silverman-Handmaker type in a family of Druze Lebanese ethnicity.
我们报告了一名男婴,其出生时具有临床和影像学证据,显示为一种致命形式的节段分化不良,与Silverman-Handmaker型不同,该男婴存活了八个多月。他有眼部和中枢神经系统异常,此前未曾有过描述。他的病程包括严重的喂养和呼吸困难、严重的身体和精神运动发育迟缓,以及病因不明的反复发热,据信发热源于中枢。该婴儿相对较长的存活期使我们能够关注这种罕见综合征的自然病史。该婴儿的父母是黎巴嫩德鲁兹族近亲,这支持了该病的常染色体隐性遗传模式。这是黎巴嫩德鲁兹族家族中首次记录到Silverman-Handmaker型节段分化不良。