Literature DB >> 20084395

Lethal epiphyseal stippling in the foetus and neonate; pathological implications.

Helen Wainwright1, Peter Beighton.   

Abstract

Autopsy reports accumulated since 1991 contained 30 cases in which routine radiological investigation had demonstrated radio-dense stippling of the epiphyses. The case histories, pregnancy progress, clinical manifestations, cytogenetic investigations, and autopsy findings have been tabulated and analysed for the purpose of diagnostic discrimination. Firm diagnoses were obtained in eight instances: warfarin embryopathy-three, trisomy 18-three, lethal multiple pterygium syndrome-one. Other possible but unconfirmed diagnoses were chromosomal aneuploidy-three, sonic hedgehog phenotype-one, CHARGE association-one, intrauterine infection-one. The value of autopsy in foetuses and neonates with lethal epiphyseal stippling syndromes is exemplified by the detection of multiple visceral abnormalities in ten instances.

Entities:  

Mesh:

Year:  2010        PMID: 20084395     DOI: 10.1007/s00428-009-0877-9

Source DB:  PubMed          Journal:  Virchows Arch        ISSN: 0945-6317            Impact factor:   4.064


  14 in total

Review 1.  Chondrodysplasia punctata and maternal autoimmune disease: a new case and review of the literature.

Authors:  Alan L Shanske; Larry Bernstein; Ronit Herzog
Journal:  Pediatrics       Date:  2007-08       Impact factor: 7.124

2.  Multiple malformations: a possible Sonic hedgehog phenotype?

Authors:  Helen Wainwright; Peter Beighton
Journal:  Virchows Arch       Date:  2009-02-10       Impact factor: 4.064

Review 3.  Chondrodysplasia punctata: a clinical diagnostic and radiological review.

Authors:  Melita D Irving; Lyn S Chitty; Sahar Mansour; Christine M Hall
Journal:  Clin Dysmorphol       Date:  2008-10       Impact factor: 0.816

4.  Chondrodysplasia punctata and maternal systemic lupus erythematosus.

Authors:  H V Toriello
Journal:  J Med Genet       Date:  1998-08       Impact factor: 6.318

Review 5.  [Chondrodysplasia punctata associated with Down's syndrome. Presentation of a case and review of the literature].

Authors:  J Hernández; S Salas; I Pastor; J Quero; F Collado; F Omeñaca
Journal:  An Esp Pediatr       Date:  1988-02

6.  Abnormal sterol metabolism in patients with Conradi-Hünermann-Happle syndrome and sporadic lethal chondrodysplasia punctata.

Authors:  R I Kelley; W G Wilcox; M Smith; L E Kratz; A Moser; D S Rimoin
Journal:  Am J Med Genet       Date:  1999-03-19

Review 7.  Novel and recurrent EBP mutations in X-linked dominant chondrodysplasia punctata.

Authors:  S Ikegawa; H Ohashi; T Ogata; A Honda; M Tsukahara; T Kubo; M Kimizuka; M Shimode; T Hasegawa; G Nishimura; Y Nakamura
Journal:  Am J Med Genet       Date:  2000-10-02

8.  The nature of cartilage stippling in chondrodysplasia punctata: histopathological study of Conradi-Hünermann syndrome.

Authors:  Ugo Ernesto Pazzaglia; Guido Zarattini; Carla Donzelli; Anna Benetti; Maria Pia Bondioni; Caterina Groli
Journal:  Fetal Pediatr Pathol       Date:  2008       Impact factor: 0.958

9.  Conradi-Hünermann-Happle syndrome (X-linked dominant chondrodysplasia punctata) confirmed by plasma sterol and mutation analysis.

Authors:  Annette Kolb-Mäurer; Karl-Heinz Grzeschik; Dorothea Haas; Eva-Bettina Bröcker; Henning Hamm
Journal:  Acta Derm Venereol       Date:  2008       Impact factor: 4.437

10.  Prenatal testing for a novel EBP missense mutation causing X-linked dominant chondrodysplasia punctata.

Authors:  Carolyn Tysoe; Caroline J Law; Richard Caswell; Peter Clayton; Sian Ellard
Journal:  Prenat Diagn       Date:  2008-05       Impact factor: 3.050

View more
  1 in total

1.  Warfarin embryopathy: fetal manifestations.

Authors:  Helen Wainwright; Peter Beighton
Journal:  Virchows Arch       Date:  2010-10-05       Impact factor: 4.064

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.