Literature DB >> 12775540

Early manifestation of Ghosal-type hemato-diaphyseal dysplasia.

Mardawig Alebouyeh1, Parvanch Vossough, Firouz Tabarrok.   

Abstract

Ghosal-type hemato-diaphyseal dysplasia is a rare autosomal recessive disorder with distinctive diaphyseal and metaphyseal dysplasia of long bones and steroid-dependant anemia. The authors describe a 20-month-old girl who had had a severe transfusion-dependent anemia since late infancy and marked locomotion difficulties as a toddler. The diagnosis was established by X-ray bone survey. The anemia was treated with oral prednisolone. Since then, the patient has been doing well on steroid-maintenance therapy and has no more walking difficulties. The incidence of hemato-diaphyseal dysplasia in the Indian subcontinent and Middle East is notable.

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Year:  2003        PMID: 12775540

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN: 0888-0018            Impact factor:   1.969


  4 in total

1.  A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34.

Authors:  B Isidor; N Dagoneau; C Huber; D Genevieve; B Bader-Meunier; S Blanche; C Picard; M C De Vernejoul; A Munnich; M Le Merrer; V Cormier-Daire
Journal:  Hum Genet       Date:  2007-01-03       Impact factor: 4.132

2.  Ghosal Syndrome--Ten Years Follow-up.

Authors:  Rakesh Mondal; Archan Sil; Shankha Subhra Nag; Tapas Sabui
Journal:  Indian J Pediatr       Date:  2015-01-20       Impact factor: 1.967

Review 3.  Ghosal hematodiaphyseal dysplasia-a concise review including an illustrative patient.

Authors:  Richa Arora; Shagun Aggarwal; Swaroopa Deme
Journal:  Skeletal Radiol       Date:  2014-08-30       Impact factor: 2.199

Review 4.  Ghosal type hemato-diaphyseal dysplasia: a rare variety of Engelmann's disease.

Authors:  R K Mondal; B Karmakar; P K Chandra; K Mukherjee
Journal:  Indian J Pediatr       Date:  2007-03       Impact factor: 5.319

  4 in total

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