Literature DB >> 3130853

Geleophysic dysplasia--acromicric dysplasia with evidence of glycoprotein storage.

A H Lipson1, A E Kan, K Kozlowski.   

Abstract

"Geleophysic" dysplasia is a rare autosomal recessive disorder, probably of glycoprotein metabolism, which shares some clinical and roentgenological manifestations with acromicric dysplasia. We report the clinical, radiological, and pathological data of a patient with the typical picture of progressive growth delay; mild facial anomalies; small, abnormal hands; hepatosplenomegaly; and progressive cardiac valvular lesions. Electron microscopy of a liver biopsy showed similar and additional changes to those published previously.

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Year:  1987        PMID: 3130853     DOI: 10.1002/ajmg.1320280522

Source DB:  PubMed          Journal:  Am J Med Genet Suppl        ISSN: 1040-3787


  3 in total

1.  Acromicric dysplasia and geleophysic dysplasia: similarities and differences.

Authors:  R C Hennekam; Y van Bever; J W Oorthuys
Journal:  Eur J Pediatr       Date:  1996-04       Impact factor: 3.183

2.  Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance.

Authors:  L Faivre; M Le Merrer; C Baumann; M Polak; P Chatelain; V Sulmont; J Cousin; M Bost; M P Cordier; E Zackai; K Russell; G Finidori; J C Pouliquen; A Munnich; P Maroteaux; V Cormier-Daire
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

3.  Skin fibroblasts of patients with geleophysic dysplasia due to FBN1 mutations have lysosomal inclusions and losartan improves their microfibril deposition defect.

Authors:  Pasquale Piccolo; Valeria Sabatino; Pratibha Mithbaokar; Elena Polishchuk; John Hicks; Roman Polishchuk; Carlos A Bacino; Nicola Brunetti-Pierri
Journal:  Mol Genet Genomic Med       Date:  2019-07-27       Impact factor: 2.183

  3 in total

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