Literature DB >> 8444237

Restrictive dermopathy: a lethal congenital skin disorder.

R Hoffmann1, M Lohner, N Böhm, J Leititis, H Helwig.   

Abstract

Restrictive dermopathy is a recently described lethal congenital disorder of the skin with an autosomal recessive mode of inheritance. The rigidity of the skin impairs fetal movements in utero and causes arthrogryposis, as well as highly characteristic facial features and pulmonary hypoplasia. We report two cases of restrictive dermopathy in prematurely born infants, describe the typical pathological findings and discuss this disorder in the context of the fetal akinesia/hypokinesia deformation sequence.

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Year:  1993        PMID: 8444237     DOI: 10.1007/bf02072481

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  23 in total

1.  Restrictive dermopathy: a newly recognized autosomal recessive skin dysplasia.

Authors:  D R Witt; M R Hayden; K A Holbrook; B A Dale; V J Baldwin; G P Taylor
Journal:  Am J Med Genet       Date:  1986-08

Review 2.  Analysis of Pena Shokeir phenotype.

Authors:  J G Hall
Journal:  Am J Med Genet       Date:  1986-09

3.  Epithelial character and morphologic diversity of cell cultures from human amniotic fluids examined by immunofluorescence microscopy and gel electrophoresis of cytoskeletal proteins.

Authors:  B A Ochs; W W Franke; R Moll; C Grund; M Cremer; T Cremer
Journal:  Differentiation       Date:  1983       Impact factor: 3.880

4.  Congenital skin defects and gastrointestinal atresia.

Authors:  N J Leschot
Journal:  Am J Med Genet       Date:  1983-05

5.  Autosomal-recessive aplasia cutis congenita--report of two affected sibs.

Authors:  H V Toriello; J V Higgins; D F Waterman
Journal:  Am J Med Genet       Date:  1983-05

6.  Restrictive dermopathy with distinct morphological abnormalities.

Authors:  M Van Hoestenberghe; E Legius; W Vandevoorde; A Eykens; J Jaeken; E Eggermont; R Devos; C De Wolf-Peeters; J P Fryns
Journal:  Am J Med Genet       Date:  1990-07

7.  Aplasia cutis congenita in two sibs discordant for pyloric atresia.

Authors:  R Carmi; S Sofer; M Karplus; Y Ben-Yakar; D Mahler; H Zirkin; J Bar-Ziv
Journal:  Am J Med Genet       Date:  1982-03

8.  Restrictive dermopathy in two brothers.

Authors:  R Happle; J H Stekhoven; B C Hamel; L A Kollée; J G Nijhuis; I Anton-Lamprecht; P M Steijlen
Journal:  Arch Dermatol       Date:  1992-02

9.  Severe congenital skin defects in a newborn. Case report and relevance of several obstetrical parameters.

Authors:  N J Leschot; P E Treffers; M J Becker-Bloemkolk; S van Zanten; W P de Groot; M Verjaal
Journal:  Eur J Obstet Gynecol Reprod Biol       Date:  1980-07       Impact factor: 2.435

Review 10.  Genetically induced abnormalities of epidermal differentiation and ultrastructure in ichthyoses and epidermolyses: pathogenesis, heterogeneity, fetal manifestation, and prenatal diagnosis.

Authors:  I Anton-Lamprecht
Journal:  J Invest Dermatol       Date:  1983-07       Impact factor: 8.551

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  3 in total

Review 1.  Diseases of the Nucleoskeleton.

Authors:  James M Holaska
Journal:  Compr Physiol       Date:  2016-09-15       Impact factor: 9.090

2.  Restrictive dermopathy.

Authors:  M H Reed; A E Chudley; M Kroeker; D M Wilmot
Journal:  Pediatr Radiol       Date:  1993

3.  Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development.

Authors:  Casey L Moulson; Daniel R Martin; Jesse J Lugus; Jean E Schaffer; Anne C Lind; Jeffrey H Miner
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-15       Impact factor: 11.205

  3 in total

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