RT Journal Article SR Electronic T1 Growth hormone deficiency and empty sella in DIDMOAD syndrome: an endocrine study. JF Archives of Disease in Childhood JO Arch Dis Child FD BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health SP 251 OP 253 DO 10.1136/adc.73.3.251 VO 73 IS 3 A1 A T Soliman A1 B Bappal A1 A Darwish A1 A Rajab A1 M Asfour YR 1995 UL http://adc.bmj.com/content/73/3/251.abstract AB 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.