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Familial ichthyosis, dwarfism, mental retardation, and renal disease.

作者信息

Rayner A, Lampert R P, Rennert O M

出版信息

J Pediatr. 1978 May;92(5):766-8. doi: 10.1016/s0022-3476(78)80146-2.

DOI:10.1016/s0022-3476(78)80146-2
PMID:641625
Abstract

The nonrandom association of congenital ichthyosis with neurologic impairment, ectodermal dysplasia, dwarfism, hypogonadism, and renal disease has prompted the review of numerous syndromes. The difficulties in characterization of syndromes in the absence of pathognomonic signs is discussed in relation to three siblings presented herein. Despite extensive investigation, underlying metabolic defects remain obscure.

摘要

相似文献

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Familial ichthyosis, dwarfism, mental retardation, and renal disease.
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引用本文的文献

1
End-stage renal failure in a child with X-linked ichthyosis.一名患有X连锁鱼鳞病的儿童的终末期肾衰竭。
Pediatr Nephrol. 2003 Mar;18(3):297-300. doi: 10.1007/s00467-002-1042-8. Epub 2003 Feb 7.
2
Genetic heterogeneity of the ichthyosis, hypogonadism, mental retardation, and epilepsy syndrome. Clinical and biochemical investigations on two patients with Rud syndrome and review of the literature.鱼鳞病、性腺功能减退、智力发育迟缓及癫痫综合征的遗传异质性。对两名Rud综合征患者的临床及生化研究并文献复习。
Eur J Pediatr. 1983 Oct;141(1):8-13. doi: 10.1007/BF00445661.
3
Fanconi syndrome, ichthyosis, dysmorphism, jaundice and diarrhoea--a new syndrome.
范科尼综合征、鱼鳞病、畸形、黄疸和腹泻——一种新综合征。
Pediatr Nephrol. 1990 Jul;4(4):308-13. doi: 10.1007/BF00862505.