Literature DB >> 7358236

Marble brain disease: recessive osteopetrosis, renal tubular acidosis and cerebral calcification in three Saudi Arabian families.

A Ohlsson, G Stark, N Sakati.   

Abstract

Four children are described from three Saudi Arabian families suffering from osteopetrosis, distal renal tubular acidosis and cerebral calcification associated clinically with mental retardation, stunted growth, abnormal teeth and a similar facial appearance. The syndrome is inherited as an autosomal recessive. The growth retardation is attributed to renal tubular acidosis but no metabolic link is evident between its other major features, and the fundamental defect is unknown. The disorder is radiologically indistinguishable from the classical recessive (malignant) and dominant (benign) forms of osteopetrosis but its other characteristics establish it as a separate disease entity.

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Year:  1980        PMID: 7358236     DOI: 10.1111/j.1469-8749.1980.tb04307.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  15 in total

Review 1.  Variable clinical presentation of carbonic anhydrase deficiency: evidence for heterogeneity?

Authors:  P Strisciuglio; R Sartorio; C Pecoraro; F Lotito; W S Sly
Journal:  Eur J Pediatr       Date:  1990-02       Impact factor: 3.183

2.  Carbonic anhydrase II deficiency: report of a novel mutation.

Authors:  Aynaa Alsharidi; Mohammad Al-Hamed; Abdulkareem Alsuwaida
Journal:  CEN Case Rep       Date:  2015-12-08

Review 3.  Human chromosome 8.

Authors:  S Wood
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

4.  The association of infantile osteopetrosis and neuronal storage disease in two brothers.

Authors:  V Jagadha; W C Halliday; L E Becker; D Hinton
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

5.  The syndrome of osteopetrosis in siblings: its occurrence in two sisters in Nigeria.

Authors:  A Adeloye
Journal:  Childs Nerv Syst       Date:  1987       Impact factor: 1.475

Review 6.  The Erlenmeyer flask bone deformity in the skeletal dysplasias.

Authors:  Maha A Faden; Deborah Krakow; Fatih Ezgu; David L Rimoin; Ralph S Lachman
Journal:  Am J Med Genet A       Date:  2009-06       Impact factor: 2.802

Review 7.  Acidosis and Urinary Calcium Excretion: Insights from Genetic Disorders.

Authors:  R Todd Alexander; Emmanuelle Cordat; Régine Chambrey; Henrik Dimke; Dominique Eladari
Journal:  J Am Soc Nephrol       Date:  2016-07-28       Impact factor: 10.121

Review 8.  Pediatric renal diseases in the Kingdom of Saudi Arabia.

Authors:  Jameela Abdulaziz Kari
Journal:  World J Pediatr       Date:  2012-08-12       Impact factor: 2.764

9.  Osteopetrosis: brain ultrasound and computed tomography findings.

Authors:  P J Patel; T M Kolawole; S al-Mofada; T M Malabarey; A Hulailah
Journal:  Eur J Pediatr       Date:  1992-11       Impact factor: 3.183

10.  Mice carrying a CAR-2 null allele lack carbonic anhydrase II immunohistochemically and show vascular calcification.

Authors:  S S Spicer; S E Lewis; R E Tashian; B A Schulte
Journal:  Am J Pathol       Date:  1989-04       Impact factor: 4.307

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