Literature DB >> 3717214

Another Italian family with mandibuloacral dysplasia: why does it seem more frequent in Italy?

R Tenconi, F Miotti, A Miotti, G Audino, R Ferro, M Clementi.   

Abstract

We describe three patients (one female and two males in a sibship of 11) with mandibuloacral dysplasia. Only eight families have been reported previously, and of these, four were of Italian origin. The phenotypic spectrum of the condition is delineated and its variability is stressed. The observation of three affected members of both sexes with normal parents supports the hypothesis of autosomal recessive inheritance. The reasons for the high frequency of the condition in Italy are discussed; a local selective advantage for heterozygotes and founder effect might be involved.

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Year:  1986        PMID: 3717214     DOI: 10.1002/ajmg.1320240215

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


  5 in total

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2.  Mandibuloacral dysplasia as a form of idiopathic osteolysis.

Authors:  J P Fryns; C Schrander-Stumpel; A Spaepen
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3.  Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C.

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4.  Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblings.

Authors:  Y Miyoshi; M Akagi; A K Agarwal; N Namba; K Kato-Nishimura; I Mohri; M Yamagata; S Nakajima; S Mushiake; M Shima; R J Auchus; M Taniike; A Garg; K Ozono
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5.  A case of craniomandibular dermatodysostosis associated with focal glomerulosclerosis.

Authors:  E Pedagogos; G Flanagan; D M Francis; G J Becker; D M Danks; R G Walker
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  5 in total

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