Literature DB >> 1259284

The clinical features of sclerosteosis. A review of the manifestations in twenty-five affected individuals.

P Beighton, L Durr, H Hamersma.   

Abstract

Sclerosteosis is a unique autosomal recessive condition in which skeletal overgrowth is associated with syndactyly and digital malformation. Analysis of the course and clinical features in 25 affected individuals showed that the condition is progressive and potentially lethal. Facial palsy and deafness are common complications and raised intracranial pressure may develop. The clinical and radiographic stigmata of sclerosteosis permit differentiation from the other disorders of the "osteopetrosis" or "Albers-Schönberg disease" group, in which bony thickening and cranial nerve palsy occur.

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Mesh:

Year:  1976        PMID: 1259284     DOI: 10.7326/0003-4819-84-4-393

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  28 in total

1.  Osteocyte control of bone formation via sclerostin, a novel BMP antagonist.

Authors:  David G Winkler; May Kung Sutherland; James C Geoghegan; Changpu Yu; Trenton Hayes; John E Skonier; Diana Shpektor; Mechtild Jonas; Brian R Kovacevich; Karen Staehling-Hampton; Mark Appleby; Mary E Brunkow; John A Latham
Journal:  EMBO J       Date:  2003-12-01       Impact factor: 11.598

Review 2.  Sclerosing bone dysplasias--a target-site approach.

Authors:  A Greenspan
Journal:  Skeletal Radiol       Date:  1991       Impact factor: 2.199

3.  Sclerosteosis.

Authors:  P Beighton
Journal:  J Med Genet       Date:  1988-03       Impact factor: 6.318

4.  Fatal cerebellar herniation secondary to Camurati-Englemann's disease.

Authors:  R K Simpson; D K Fischer; G K Gall; J E Rose
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-10       Impact factor: 10.154

Review 5.  Craniotubular bone disorders.

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

6.  Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21.

Authors:  W Balemans; J Van Den Ende; A Freire Paes-Alves; F G Dikkers; P J Willems; F Vanhoenacker; N de Almeida-Melo; C F Alves; C A Stratakis; S C Hill; W Van Hul
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

7.  High-bone-mass-producing mutations in the Wnt signaling pathway result in distinct skeletal phenotypes.

Authors:  Paul J Niziolek; Takeisha L Farmer; Yajun Cui; Charles H Turner; Matthew L Warman; Alexander G Robling
Journal:  Bone       Date:  2011-08-09       Impact factor: 4.398

Review 8.  Wnt modulators in the biotech pipeline.

Authors:  Jean-Philippe Rey; Debra L Ellies
Journal:  Dev Dyn       Date:  2010-01       Impact factor: 3.780

9.  Sclerosteosis in a Spanish male: first report in a person of Mediterranean origin.

Authors:  M Bueno; G Oliván; A Jiménez; J M Garagorri; A Sarría; A L Bueno; M Bueno; F J Ramos
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

Review 10.  A review of the osteopetroses.

Authors:  P Beighton; F Horan; H Hamersma
Journal:  Postgrad Med J       Date:  1977-08       Impact factor: 2.401

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