Literature DB >> 7405956

Osteopathia striata associated with familial dermopathy and white forelock: evidence for postnatal development of osteopathia striata.

M P Whyte, W A Murphy.   

Abstract

Osteopathia striata and a macular, hyperpigmented dermopathy were found in a Caucasian woman and her two daughters. Sequential radiographs in one daughter showed that the bone lesions were not present during infancy but developed during early childhood. The skin lesions were not those most often associated with osteopathia striata, but appeared tgo be a unique dermatosis, which also included a hypopigmented forelock. A son had neither osseous nor ectodermal lesions. These abnormalities appear to represent a new syndrome, which is inherited with X-linked or autosomal dominant transmission.

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Year:  1980        PMID: 7405956     DOI: 10.1002/ajmg.1320050303

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  Mixed-sclerosing-bone-dystrophy: 42-year follow-up of a case reported as osteopetrosis.

Authors:  R Pacifici; W A Murphy; S L Teitelbaum; M P Whyte
Journal:  Calcif Tissue Int       Date:  1986-03       Impact factor: 4.333

2.  Mixed-sclerosing-bone-dystrophy: report of a case and review of the literature.

Authors:  M P Whyte; W A Murphy; M D Fallon; T J Hahn
Journal:  Skeletal Radiol       Date:  1981       Impact factor: 2.199

Review 3.  Osteopathia striata with cranial sclerosis.

Authors:  B B Gay; L J Elsas; J B Wyly; M Pasquali
Journal:  Pediatr Radiol       Date:  1994
  3 in total

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