Literature DB >> 8091333

Congenital cutis laxa with a dominant inheritance and early onset emphysema.

E Corbett1, H Glaisyer, C Chan, B Madden, A Khaghani, M Yacoub.   

Abstract

Two cases (mother and daughter) are reported of autosomal dominant cutis laxa which are unusual in being associated with early onset emphysema. Both mother and daughter have been smokers and are heterozygotes for the alpha 1 antitrypsin genotype. The combination of cigarette smoking and subnormal alpha 1 antitrypsin levels may explain the pulmonary spread in these two women who have what is usually a benign form of cutis laxa limited to the skin.

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Year:  1994        PMID: 8091333      PMCID: PMC475135          DOI: 10.1136/thx.49.8.836

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  7 in total

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Authors:  L CHRISTIAENS; A MARCHAND-ALPHANT; A FOVET
Journal:  Presse Med       Date:  1954-12-25       Impact factor: 1.228

2.  Acquired cutis laxa (generalized elastolysis): light and electron microscopic studies.

Authors:  H Nanko; L V Jepsen; H Zachariae; H Søgaard
Journal:  Acta Derm Venereol       Date:  1979       Impact factor: 4.437

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Journal:  Clin Genet       Date:  1986-02       Impact factor: 4.438

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Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318

5.  Cutis laxa. A manifestation of generalized elastolysis.

Authors:  R W Goltz; A M Hult; M Goldfarb; R J Gorlin
Journal:  Arch Dermatol       Date:  1965-10

6.  X-linked cutis laxa: defective cross-link formation in collagen due to decreased lysyl oxidase activity.

Authors:  P H Byers; R C Siegel; K A Holbrook; A S Narayanan; P Bornstein; J G Hall
Journal:  N Engl J Med       Date:  1980-07-10       Impact factor: 91.245

7.  Emphysema and cutis laxa.

Authors:  L Turner-Stokes; C Turton; F M Pope; M Green
Journal:  Thorax       Date:  1983-10       Impact factor: 9.139

  7 in total
  7 in total

Review 1.  Progress in chronic obstructive pulmonary disease genetics.

Authors:  Edwin K Silverman
Journal:  Proc Am Thorac Soc       Date:  2006-07

2.  A functional mutation in the terminal exon of elastin in severe, early-onset chronic obstructive pulmonary disease.

Authors:  Cassandra M Kelleher; Edwin K Silverman; Thomas Broekelmann; Augusto A Litonjua; Melvin Hernandez; Jody S Sylvia; Joan Stoler; John J Reilly; Harold A Chapman; Frank E Speizer; Scott T Weiss; Robert P Mecham; Benjamin A Raby
Journal:  Am J Respir Cell Mol Biol       Date:  2005-08-04       Impact factor: 6.914

Review 3.  Emerging mechanisms of elastin transcriptional regulation.

Authors:  Sara S Procknow; Beth A Kozel
Journal:  Am J Physiol Cell Physiol       Date:  2022-07-11       Impact factor: 5.282

Review 4.  National Emphysema Treatment Trial state of the art: genetics of emphysema.

Authors:  Craig P Hersh; Dawn L DeMeo; Edwin K Silverman
Journal:  Proc Am Thorac Soc       Date:  2008-05-01

5.  Analysis of exonic elastin variants in severe, early-onset chronic obstructive pulmonary disease.

Authors:  Michael H Cho; Dawn M Ciulla; Barbara J Klanderman; Craig P Hersh; Augusto A Litonjua; David Sparrow; Benjamin A Raby; Edwin K Silverman
Journal:  Am J Respir Cell Mol Biol       Date:  2008-11-21       Impact factor: 6.914

Review 6.  Ring Finger Protein 213 in Moyamoya Disease With Pulmonary Arterial Hypertension: A Mini-Review.

Authors:  Yuting Luo; Zhixin Cao; Shaoqing Wu; Xunsha Sun
Journal:  Front Neurol       Date:  2022-03-24       Impact factor: 4.003

7.  A novel elastin gene frameshift mutation in a Russian family with cutis laxa: a case report.

Authors:  E G Okuneva; A A Kozina; N V Baryshnikova; A Yu Krasnenko; K Yu Tsukanov; O I Klimchuk; E I Surkova; V V Ilinsky
Journal:  BMC Dermatol       Date:  2019-01-31
  7 in total

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