Literature DB >> 1789294

Cartilage hair hypoplasia, metaphyseal chondrodysplasia type McKusick: description of seven patients and review of the literature.

I van der Burgt1, A Haraldsson, J C Oosterwijk, A J van Essen, C Weemaes, B Hamel.   

Abstract

We describe 7 cases of cartilage hair hypoplasia (CHH) with emphasis on the clinical and immunological aspects. The literature on CHH is reviewed and symptoms in 63 non-Amish cases are summarized. In this autosomal recessive disorder the immunodeficiency, hair abnormalities, and severity of skeletal involvement show extremely variable expressivity, between and within families. Two of the 3 sib-pairs among our cases demonstrate the great difference in expression within one family. At adult age roentgenological abnormalities can be very mild, or even absent. An impairment in cell-mediated immunity is present in all of our cases and seems a consistent manifestation in CHH; however, sometimes it is very subtle and without clinical symptoms.

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Mesh:

Year:  1991        PMID: 1789294     DOI: 10.1002/ajmg.1320410320

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  13 in total

Review 1.  Primary T-lymphocyte immunodeficiencies.

Authors:  A Fischer
Journal:  Clin Rev Allergy Immunol       Date:  2001-02       Impact factor: 8.667

2.  Cartilage-hair hypoplasia syndrome: increased apoptosis of T lymphocytes is associated with altered expression of Fas (CD95), FasL (CD95L), IAP, Bax, and Bcl2.

Authors:  L Yel; S Aggarwal; S Gupta
Journal:  J Clin Immunol       Date:  1999-11       Impact factor: 8.317

3.  Bone marrow transplantation in cartilage-hair hypoplasia: correction of the immunodeficiency but not of the chondrodysplasia.

Authors:  F Berthet; C A Siegrist; H Ozsahin; P Tuchschmid; G Eich; A Superti-Furga; R A Seger
Journal:  Eur J Pediatr       Date:  1996-04       Impact factor: 3.183

Review 4.  Cartilage-hair hypoplasia.

Authors:  O Mäkitie; T Sulisalo; A de la Chapelle; I Kaitila
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

5.  Low segregation ratios in autosomal recessive disorders.

Authors:  J C Oosterwijk
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

6.  Small RNAs derived from lncRNA RNase MRP have gene-silencing activity relevant to human cartilage-hair hypoplasia.

Authors:  Leslie E Rogler; Brian Kosmyna; David Moskowitz; Remon Bebawee; Joseph Rahimzadeh; Katrina Kutchko; Alain Laederach; Luigi D Notarangelo; Silvia Giliani; Eric Bouhassira; Paul Frenette; Jayanta Roy-Chowdhury; Charles E Rogler
Journal:  Hum Mol Genet       Date:  2013-09-05       Impact factor: 6.150

7.  Defective in-vitro colony formation of haematopoietic progenitors in patients with cartilage-hair hypoplasia and history of anaemia.

Authors:  E Juvonen; O Mäkitie; A Mäkipernaa; T Ruutu; I Kaitila; J Rajantie
Journal:  Eur J Pediatr       Date:  1995-01       Impact factor: 3.183

8.  A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9.

Authors:  M Bamshad; W S Watkins; R K Zenger; J F Bohnsack; J C Carey; B Otterud; P A Krakowiak; M Robertson; L B Jorde
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

9.  Genetic homogeneity of cartilage-hair hypoplasia.

Authors:  T Sulisalo; I van der Burgt; D L Rimoin; J Bonaventure; D Sillence; J B Campbell; D Chitayat; C I Scott; A de la Chapelle; P Sistonen
Journal:  Hum Genet       Date:  1995-02       Impact factor: 4.132

Review 10.  Educational paper: syndromic forms of primary immunodeficiency.

Authors:  Rogier Kersseboom; Alice Brooks; Corry Weemaes
Journal:  Eur J Pediatr       Date:  2011-02-22       Impact factor: 3.183

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