Literature DB >> 641625

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

A Rayner, R P Lampert, O M Rennert.   

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.

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Year:  1978        PMID: 641625     DOI: 10.1016/s0022-3476(78)80146-2

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  3 in total

1.  Fanconi syndrome, ichthyosis, dysmorphism, jaundice and diarrhoea--a new syndrome.

Authors:  J E Deal; T M Barratt; M J Dillon
Journal:  Pediatr Nephrol       Date:  1990-07       Impact factor: 3.714

2.  End-stage renal failure in a child with X-linked ichthyosis.

Authors:  Hiro Matsukura; Tatsuya Fuchizawa; Akio Ohtsuki; Hiroyuki Higashiyama; Osamu Higuchi; Akira Higuchi; Toshio Miyawaki
Journal:  Pediatr Nephrol       Date:  2003-02-07       Impact factor: 3.714

3.  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.

Authors:  M Münke; K Kruse; M Goos; H H Ropers; M Tolksdorf
Journal:  Eur J Pediatr       Date:  1983-10       Impact factor: 3.183

  3 in total

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