Literature DB >> 2754071

Cutis laxa with ultrastructural abnormalities of elastic fiber.

Y Kitano1, K Nishida, N Okada, T Mimaki, H Yabuuchi.   

Abstract

A case of a congenital, autosomal recessive form of generalized cutis laxa is reported. The patient was a 27-month-old boy with generalized flaccid skin and short stature. Radiologic examination revealed that the age of the bones of the wrist was compatible with a chronologic age of only 1 year. Elastic fibers were diminished throughout the dermis, and results of electron microscopic study showed globular and unstained elastin and relatively large amounts of the microfibrillar components of elastic fibers.

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Year:  1989        PMID: 2754071     DOI: 10.1016/s0190-9622(89)80039-8

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  2 in total

1.  Genetic heterogeneity of cutis laxa: a heterozygous tandem duplication within the fibulin-5 (FBLN5) gene.

Authors:  Dessislava Markova; Yaqun Zou; Franziska Ringpfeil; Takako Sasaki; Günter Kostka; Rupert Timpl; Jouni Uitto; Mon-Li Chu
Journal:  Am J Hum Genet       Date:  2003-02-28       Impact factor: 11.025

2.  Congenital cutis laxa.

Authors:  Anupama Mauskar; Preeti Shanbag; Varsha Ahirrao; Leena Nagotkar
Journal:  Ann Saudi Med       Date:  2010 Mar-Apr       Impact factor: 1.526

  2 in total

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