Literature DB >> 6846273

Congenital cutis laxa and osteoporosis.

N O Sakati, W L Nyhan.   

Abstract

A 16-month-old male infant was studied who had a syndrome of cutis laxa and incapacitating osteoporosis. The bones displayed evidence of multiple fractures, with impaction and deformities even in the absence of weight bearing. In addition, the infant had large ears and antimongoloid obliquity of the palpebral fissures.

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Year:  1983        PMID: 6846273     DOI: 10.1001/archpedi.1983.02140310034008

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  4 in total

1.  Collagen studies in congenital cutis laxa.

Authors:  A Taïeb; M Aumailley; D Courouge-Dorcier; M Rabaud; P Bioulac-Sage; J E Surlève-Bazeille; J Maleville
Journal:  Arch Dermatol Res       Date:  1987       Impact factor: 3.017

2.  Is geroderma osteodysplastica underdiagnosed?

Authors:  A G Hunter
Journal:  J Med Genet       Date:  1988-12       Impact factor: 6.318

3.  Congenital cutis laxa with retardation of growth and development.

Authors:  M A Patton; J Tolmie; P Ruthnum; S Bamforth; M Baraitser; M Pembrey
Journal:  J Med Genet       Date:  1987-09       Impact factor: 6.318

4.  Osteoporosis is a neglected health priority in Arab World: a comparative bibliometric analysis.

Authors:  Waleed M Sweileh; Samah W Al-Jabi; Sa'ed H Zyoud; Ansam F Sawalha; Mustafa A Ghanim
Journal:  Springerplus       Date:  2014-08-12
  4 in total

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