Literature DB >> 7492167

Growth hormone deficiency and empty sella in DIDMOAD syndrome: an endocrine study.

A T Soliman1, B Bappal, A Darwish, A Rajab, M Asfour.   

Abstract

Two girls with DIDMOAD syndrome are presented. One also had severe megaloblastic-sideroblastic anaemia and the other several neurological manifestations. Both were short with defective growth hormone secretion. Computed tomography revealed empty sella in both girls; one had widespread atrophic cortical and cerebellar changes. High doses of thiamine improved the anaemia in the first case, increased C peptide secretion in both, but had no effect on the neurological abnormalities.

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Year:  1995        PMID： 7492167      PMCID： PMC1511277          DOI： 10.1136/adc.73.3.251

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


  6 in total

1.  SIDEROBLASTIC ANAEMIA IN MAN: OBSERVATIONS ON SEVENTY CASES.

Authors:  B H MACGIBBON; D L MOLLIN
Journal:  Br J Haematol       Date:  1965-01       Impact factor: 6.998

2.  Coexistence of diabetes mellitus and insipidus and optic atrophy in two male siblings. Studies and review of literature.

Authors:  G W Bretz; A Baghdassarian; J D Graber; B J Zacherle; R A Norum; R M Blizzard
Journal:  Am J Med       Date:  1970-03       Impact factor: 4.965

3.  Association of juvenile diabetes mellitus, primary optic atrophy and perceptive hearing loss in three sibs, with additional idiopathic diabetes mellitus insipidus in one case.

Authors:  D G Ikkos; G R Fraser; E Matsouki-Gavra; M Petrochilos
Journal:  Acta Endocrinol (Copenh)       Date:  1970-09

4.  Thiamine-responsive anemia in DIDMOAD syndrome.

Authors:  C Borgna-Pignatti; P Marradi; L Pinelli; N Monetti; C Patrini
Journal:  J Pediatr       Date:  1989-03       Impact factor: 4.406

5.  Wolfram syndrome: report of four new cases and a review of literature.

Authors:  L Fishman; R M Ehrlich
Journal:  Diabetes Care       Date:  1986 Jul-Aug       Impact factor: 19.112

6.  Juvenile diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, atonia of the urinary tract and bladder, and other abnormalities (Wolfram syndrome). A review of 88 cases from the literature with personal observations on 3 new patients.

Authors:  C W Cremers; P G Wijdeveld; A J Pinckers
Journal:  Acta Paediatr Scand Suppl       Date:  1977
  6 in total
  4 in total

1.  Wolfram syndrome: a clinicopathologic correlation.

Authors:  Justin B Hilson; Saumil N Merchant; Joe C Adams; Jeffrey T Joseph
Journal:  Acta Neuropathol       Date:  2009-05-16       Impact factor: 17.088

2.  The novel compound heterozygous mutations, V434del and W666X, in WFS1 gene causing the Wolfram syndrome in a Chinese family.

Authors:  Jie Hong; Yu-Wen Zhang; Hui-Jie Zhang; Hui-Ying Jia; Yu Zhang; Xiao-Yi Ding; Dan-Yang Zhou; Hui-Ping Chen; Xiao-Hua Jiang; Bin Cui; Xiao-Ying Li; Guang Ning
Journal:  Endocrine       Date:  2009-01-22       Impact factor: 3.633

3.  Empty sella syndrome in a male child with failure to thrive.

Authors:  Debasmita Rath; Ranjan Kumar Sahoo; Jasashree Choudhury; Dillip Kumar Dash; Anuspandana Mohapatra
Journal:  J Pediatr Neurosci       Date:  2015 Jan-Mar

4.  Diabetes mellitus, diabetes insipidus, optic atrophy, and deafness: A case of Wolfram (DIDMOAD) syndrome.

Authors:  Nasrollah Maleki; Bahman Bashardoust; Anahita Zakeri; Azita Salehifar; Zahra Tavosi
Journal:  J Curr Ophthalmol       Date:  2016-01-02
  4 in total

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