Literature DB >> 6721654

[Congenital familial dwarfism with cephaloskeletal dysplasia (Taybi-Linder syndrome)].

B Lavollay, C Faure, G Filipe, G Branca, Y Huet de Barochez.   

Abstract

The authors report the case of an infant presenting with a syndrome associating dwarfism, microcephaly, facial dysmorphy and important skeletal abnormalities consisting of radiologic changes concerning the skull, long bones, vertebrae, pelvis, ribs, metacarpus and metatarsus. Severe cerebral atrophy and neurologic involvement were responsible for death in the first year of life. This rare syndrome is likely to have an autosomal recessive transmission.

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Mesh:

Year:  1984        PMID: 6721654

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN: 0003-9764


  5 in total

1.  Cephalo-skeletal dysplasia and microcephalic osteodysplastic primordial dwarfism.

Authors:  H Taybi
Journal:  Pediatr Radiol       Date:  1992

2.  Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

Authors:  R Nagy; H Wang; B Albrecht; D Wieczorek; G Gillessen-Kaesbach; E Haan; P Meinecke; A de la Chapelle; J A Westman
Journal:  Clin Genet       Date:  2011-08-28       Impact factor: 4.438

3.  Neonatal cholestasis and focal medullary dysplasia of the kidneys in a case of microcephalic osteodysplastic primordial dwarfism.

Authors:  A Berger; N Haschke; C Kohlhauser; G Amman; U Unterberger; M Weninger
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

4.  A new syndrome with cerebro-oculo-skeletal-renal involvement.

Authors:  M C Silengo; M Lerone; A Pelizza; R Gatti; A Barabino; G Romeo
Journal:  Pediatr Radiol       Date:  1990

5.  Microcephalic osteodysplastic primordial dwarfism type I/III in sibs.

Authors:  P Meinecke; E Passarge
Journal:  J Med Genet       Date:  1991-11       Impact factor: 6.318

  5 in total

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