Literature DB >> 11260604

Prenatal diagnosis of malignant osteopetrosis in Bedouin families by linkage analysis.

H Shalev1, A Mishori-Dery, J Kapelushnik, A Moser, V C Sheffield, A McClain, R Carmi.   

Abstract

Autosomal recessive malignant osteopetrosis (MOP) is a lethal disease, unless bone marrow is successfully transplanted. Yet a donor may not always be available, and even when there is one transplantation results are far from optimal. The difficulty in obtaining conclusive results by sonographic and X-ray evaluation of the fetus makes prenatal molecular diagnosis highly desirable. Subsequent to the chromosomal localization of the MOP gene in Arab-Bedouin families from the Negev region in Israel, linkage analysis was used for the prenatal diagnosis of this disease in Bedouin families at risk. Twelve cases were diagnosed, three fetuses were found to be affected, and one of the pregnancies was terminated. The other two pregnancies continued to term and the diagnosis of osteopetrosis was confirmed by X-ray immediately after birth. This is the first report on prenatal diagnosis of autosomal recessive osteopetrosis by linkage analysis. Copyright 2001 John Wiley & Sons, Ltd.

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Year:  2001        PMID: 11260604

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  3 in total

1.  DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinity.

Authors:  Ching-Wan Lam; Sui-Fan Tong; Keong Wong; Y F Luo; Hoi-Yin Tang; Shau-Yin Ha; Michael Ho-Ming Chan
Journal:  J Hum Genet       Date:  2006-10-11       Impact factor: 3.172

2.  Osteopetrosis in pregnancy: a rare case report.

Authors:  Michaela Peer; Keelin O'Donoghue
Journal:  Obstet Med       Date:  2011-11-22

3.  Osteopetrosis with Arnold Chiari malformation type I and brain stem compression.

Authors:  M L Kulkarni; S N Marakkanavar; S Sushanth; N Pradeep; C Ashok; M D Balaji; K P Sajith; G Srinivas
Journal:  Indian J Pediatr       Date:  2007-04       Impact factor: 5.319

  3 in total

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