Cutis Laxa

T. Gardeitchik, Eva Morava-Kozicz

Research output: Chapter in Book/Report/Conference proceedingChapter

4 Citations (Scopus)

Abstract

Cutis laxa (CL) is a disorder, either acquired or inherited, in which patients have wrinkled, abundant, sagging skin with abnormal elasticity, caused by abnormal structure or function of elastin or other extracellular matrix components. Skin symptoms may be associated with variable systemic involvement, especially in the dominant and in the ARCL1 forms. In the current overview, we focus on genetic forms of CL. The inherited form has a wide genetic variability, including X-linked, autosomal dominant, and autosomal recessive patterns of inheritance. Intriguingly, several of the CL syndromes are inborn errors of metabolism. The most well-known example is Menkes disease, the first metabolic disease reported with old looking, wrinkled skin. Another unique form is ARCL2A, which is a CL syndrome presenting with reversed skin aging. In contrast, the metabolic CL syndrome ARCL2B frequently presents with progeria, evolving into a CL phenotype with wrinkled skin with further aging. Neurological involvement is very common in CL syndromes, emphasizing the importance of the underlying genes in neurodevelopment and positioning this group of disorders to neurocutaneous syndromes. There are several overlapping symptoms of the diverse types of CL syndromes. However, distinctive laboratory features, such as abnormal glycosylation and specific clinical findings, as cobblestone-like dysgenesis detected by brain imaging, occipital horns on X-ray, or abnormal wrist position with contractures, are discriminative and lead to direct genetic diagnosis.

Original languageEnglish (US)
Title of host publicationBrenner's Encyclopedia of Genetics
Subtitle of host publicationSecond Edition
PublisherElsevier Inc.
Pages254-257
Number of pages4
ISBN (Electronic)9780080961569
ISBN (Print)9780123749840
DOIs
StatePublished - Feb 27 2013
Externally publishedYes

Fingerprint

Cutis Laxa
skin (animal)
Skin
signs and symptoms (animals and humans)
Menkes disease
Aging of materials
inherited metabolic diseases
contracture
Glycosylation
elastin
neurodevelopment
Elastin
metabolic diseases
glycosylation
elasticity (mechanics)
extracellular matrix
Metabolism
Progeria
Menkes Kinky Hair Syndrome
Neurocutaneous Syndromes

Keywords

  • ATP6V0A2
  • CDG
  • Cobblestone-like brain dysgenesis
  • Cutis laxa
  • Elastin
  • Extracellular matrix
  • Fibulin-5
  • Glycosylation
  • Golgi apparatus
  • Inborn errors of metabolism
  • MAP kinase pathway
  • Mitochondrial function
  • PYCR1
  • Wrinkly skin

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Gardeitchik, T., & Morava-Kozicz, E. (2013). Cutis Laxa. In Brenner's Encyclopedia of Genetics: Second Edition (pp. 254-257). Elsevier Inc.. https://doi.org/10.1016/B978-0-12-374984-0.00367-3

Cutis Laxa. / Gardeitchik, T.; Morava-Kozicz, Eva.

Brenner's Encyclopedia of Genetics: Second Edition. Elsevier Inc., 2013. p. 254-257.

Research output: Chapter in Book/Report/Conference proceedingChapter

Gardeitchik, T & Morava-Kozicz, E 2013, Cutis Laxa. in Brenner's Encyclopedia of Genetics: Second Edition. Elsevier Inc., pp. 254-257. https://doi.org/10.1016/B978-0-12-374984-0.00367-3
Gardeitchik T, Morava-Kozicz E. Cutis Laxa. In Brenner's Encyclopedia of Genetics: Second Edition. Elsevier Inc. 2013. p. 254-257 https://doi.org/10.1016/B978-0-12-374984-0.00367-3
Gardeitchik, T. ; Morava-Kozicz, Eva. / Cutis Laxa. Brenner's Encyclopedia of Genetics: Second Edition. Elsevier Inc., 2013. pp. 254-257
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