Literature DB >> 3829443

Osteopetrosis. A genetic and epidemiological study.

J Bollerslev.   

Abstract

By a systemic search of osteopetrosis in the county of Funen, Denmark, the prevalence was 5.5/100,000 inhabitants. The study disclosed 33 patients of whom 32 had the mild, autosomal dominant form of osteopetrosis. Two obligate carriers, who had the genotype but were not phenotypically affected, were disclosed. There was a great variation in the clinical manifestations; 39% were asymptomatic. The age of first appearance of symptoms also varied widely (8-76 years), with a tendency to increasing symptoms with aging. The frequency of fractures was low. Plasma inorganic phosphate was low in 7% of the patients, and plasma acid phosphatase was increased in 39%.

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Year:  1987        PMID: 3829443

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  15 in total

1.  Elevated serum levels of creatine kinase BB in autosomal dominant osteopetrosis type II.

Authors:  J Gram; S Antonsen; M Hørder; J Bollerslev
Journal:  Calcif Tissue Int       Date:  1991-06       Impact factor: 4.333

2.  Localization of a gene for autosomal dominant osteopetrosis (Albers-Schönberg disease) to chromosome 1p21.

Authors:  W Van Hul; J Bollerslev; J Gram; E Van Hul; W Wuyts; O Benichou; F Vanhoenacker; P J Willems
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

3.  Mapping of autosomal dominant osteopetrosis type II (Albers-Schönberg disease) to chromosome 16p13.3.

Authors:  O Bénichou; E Cleiren; J Gram; J Bollerslev; M C de Vernejoul; W Van Hul
Journal:  Am J Hum Genet       Date:  2001-07-23       Impact factor: 11.025

Review 4.  Craniotubular bone disorders.

Authors:  R J Gorlin
Journal:  Pediatr Radiol       Date:  1994

5.  Fracture patterns in malignant osteopetrosis (Albers-Schönberg disease).

Authors:  N Dahl; G Holmgren; S Holmberg; H Ersmark
Journal:  Arch Orthop Trauma Surg       Date:  1992       Impact factor: 3.067

6.  Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II).

Authors:  Zhen-Lin Zhang; Jin-Wei He; Hao Zhang; Wei-Wei Hu; Wen-Zhen Fu; Jie-Mei Gu; Jin-Bo Yu; Gao Gao; Yun-Qiu Hu; Miao Li; Yu-Juan Liu
Journal:  J Bone Miner Metab       Date:  2009-03-14       Impact factor: 2.626

7.  Type II autosomal dominant osteopetrosis: radiological features in two families containing five members with asymptomatic and uncomplicated disease.

Authors:  Anastasia Fotiadou; Maria Arvaniti; Vera Kiriakou; Ioannis Tsitouridis
Journal:  Skeletal Radiol       Date:  2009-06-23       Impact factor: 2.199

8.  Clcn7F318L/+ as a new mouse model of Albers-Schönberg disease.

Authors:  J Caetano-Lopes; S G Lessard; S Hann; K Espinoza; K S Kang; K E Lim; D J Horan; H R Noonan; D Hu; R Baron; A G Robling; M L Warman
Journal:  Bone       Date:  2017-09-20       Impact factor: 4.626

9.  Generation of the first autosomal dominant osteopetrosis type II (ADO2) disease models.

Authors:  Imranul Alam; Amie K Gray; Kang Chu; Shoji Ichikawa; Khalid S Mohammad; Marta Capannolo; Mattia Capulli; Antonio Maurizi; Maurizio Muraca; Anna Teti; Michael J Econs; Andrea Del Fattore
Journal:  Bone       Date:  2013-11-01       Impact factor: 4.398

Review 10.  Friend or foe: high bone mineral density on routine bone density scanning, a review of causes and management.

Authors:  Celia L Gregson; Sarah A Hardcastle; Cyrus Cooper; Jonathan H Tobias
Journal:  Rheumatology (Oxford)       Date:  2013-02-27       Impact factor: 7.580

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