Gerodermia osteodysplastica and wrinkly skin syndrome: are they the same?
- PMID: 11424136
- DOI: 10.1002/ajmg.1352
Gerodermia osteodysplastica and wrinkly skin syndrome: are they the same?
Abstract
Gerodermia osteodysplastica (GO) is a connective tissue disorder characterized by premature aging, wrinkled, and lax skin with reduced elasticity which is more marked on the dorsum of the hands and feet associated with hyperextensible joints and osteoporosis. The wrinkly skin syndrome (WSS) is characterized by wrinkled skin over the dorsum of the hands, feet, and abdomen; hyperextensible joints, particularly of the hands; intrauterine growth retardation; postnatal failure to thrive; and mental and developmental delay. We report on five children from two consanguineous Arab families with features overlapping both GO and WSS. All five children had similar dysmorphic facial features consisting of broad and prominent forehead, hypotelorism with epicanthal folds, prominent bulbous nose, flat malar region, and large protruding ears. All had wrinkling of the skin more marked on the dorsum of the hands, feet, and abdomen; hyperextensibility of the joints, particularly of the hands; and aged appearance. Intrauterine growth retardation, subsequent failure to thrive, developmental delay, and variable degree of osteoporosis was also present in all of them. The older three children developed progressive prognathism. We suggest that GO and WSS could represent variable manifestation of the same disorder.
Copyright 2001 Wiley-Liss, Inc.
Similar articles
-
Gerodermia osteodysplastica/wrinkly skin syndrome: report of three patients and brief review of the literature.Pediatr Dermatol. 2008 Jan-Feb;25(1):66-71. doi: 10.1111/j.1525-1470.2007.00586.x. Pediatr Dermatol. 2008. PMID: 18304158 Review.
-
Geroderma osteodysplasticum hereditaria and wrinkly skin syndrome in 22 patients from Oman.Am J Med Genet A. 2008 Apr 15;146A(8):965-76. doi: 10.1002/ajmg.a.32143. Am J Med Genet A. 2008. PMID: 18348262
-
Gerodermia osteodysplastica hereditaria: report of three affected brothers and literature review.Am J Med Genet. 1979;3(4):389-95. doi: 10.1002/ajmg.1320030410. Am J Med Genet. 1979. PMID: 474638
-
Gerodermia osteodysplastica in a Bedouin sibship: further delineation of the syndrome.Clin Dysmorphol. 1997 Jan;6(1):51-5. Clin Dysmorphol. 1997. PMID: 9018419
-
Neurological involvement in a child with the wrinkly skin syndrome.Am J Med Genet. 1999 Jan 1;82(1):31-3. Am J Med Genet. 1999. PMID: 9916839 Review.
Cited by
-
Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2.Am J Hum Genet. 2009 Jul;85(1):120-9. doi: 10.1016/j.ajhg.2009.06.008. Epub 2009 Jul 2. Am J Hum Genet. 2009. PMID: 19576563 Free PMC article.
-
Golgi glycosylation and human inherited diseases.Cold Spring Harb Perspect Biol. 2011 Sep 1;3(9):a005371. doi: 10.1101/cshperspect.a005371. Cold Spring Harb Perspect Biol. 2011. PMID: 21709180 Free PMC article. Review.
-
Mutations in PYCR1 cause cutis laxa with progeroid features.Nat Genet. 2009 Sep;41(9):1016-21. doi: 10.1038/ng.413. Epub 2009 Aug 2. Nat Genet. 2009. PMID: 19648921
-
Autosomal Recessive Cutis Laxa Type II: Report of Novel Mutation in a Child.Indian Dermatol Online J. 2017 Sep-Oct;8(5):352-354. doi: 10.4103/idoj.IDOJ_334_16. Indian Dermatol Online J. 2017. PMID: 28979870 Free PMC article.
-
Examining tissue composition, whole-bone morphology and mechanical behavior of GorabPrx1 mice tibiae: A mouse model of premature aging.J Biomech. 2017 Dec 8;65:145-153. doi: 10.1016/j.jbiomech.2017.10.018. Epub 2017 Oct 25. J Biomech. 2017. PMID: 29108851 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Research Materials
Miscellaneous