Literature DB >> 462288

Osteopetrosis in South Africa. The benign, lethal and intermediate forms.

P Beighton, H Hamersma, B J Cremin.   

Abstract

Osteopetrosis is an unusual bone disorder in which the skeleton is radiographically dense. The condition is conventionally subclassified into a benign autosomal dominant adult form and a malignant autosomal recessive variety. Among 14 affected individuals whom we have studied, 4 adults had an intermediate type of osteopetrosis in which serious complications included osteomyelitis, pathological fractures and dyshaemopoiesis. The fundamental biochemical relationship of this disorder with the classic forms of osteopetrosis is uncertain. The osteopetroses must be distinguished from other sclerosing bone conditions which have a different course and prognosis. Sclerosteosis and craniometaphyseal dysplasia, both of which occur in South Africa, are of practical importance in this context.

Entities:  

Mesh:

Year:  1979        PMID: 462288

Source DB:  PubMed          Journal:  S Afr Med J


  13 in total

Review 1.  Sclerosing bone dysplasias--a target-site approach.

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

Review 2.  Craniotubular bone disorders.

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

Review 3.  [Surgery of the nerves of the neck, nose, and ear region (except Nn. stato-acusticus and olfactorius) (author's transl)].

Authors:  A Miehlke; E Stennert; R Arold; R Chilla; H Penzholz; A Kühner; V Sturm; J Haubrich
Journal:  Arch Otorhinolaryngol       Date:  1981

4.  Late-onset Visual Loss in Osteopetrosis.

Authors:  Abdul-Majid Wangai; Sheila Waa; Maryam Wangai; Erastus Amayo; Oluoch Olunya
Journal:  Sultan Qaboos Univ Med J       Date:  2011-08-15

Review 5.  Benign osteopetrosis: a review of 42 cases showing two different patterns.

Authors:  T el-Tawil; D J Stoker
Journal:  Skeletal Radiol       Date:  1993-11       Impact factor: 2.199

6.  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

7.  Intermediate form of osteopetrosis with recessive inheritance.

Authors:  N Kaibara; I Katsuki; T Hotokebuchi; K Takagishi
Journal:  Skeletal Radiol       Date:  1982       Impact factor: 2.199

8.  The development of the teeth of the microphthalmic (mi/mi) mouse.

Authors:  S M Al-Douri; D R Johnson
Journal:  J Anat       Date:  1987-08       Impact factor: 2.610

9.  Benign osteopetrosis, in a patient with sickle-cell beta+ (beta+) thalassaemia.

Authors:  D Kassimos; G Kalteziotis; G Alafakis; Z Sinakos; C Tegos
Journal:  Clin Rheumatol       Date:  1995-07       Impact factor: 2.980

10.  Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.

Authors:  W S Sly; D Hewett-Emmett; M P Whyte; Y S Yu; R E Tashian
Journal:  Proc Natl Acad Sci U S A       Date:  1983-05       Impact factor: 11.205

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