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dc.contributor.authorCrowne, Elizabeth C
dc.contributor.authorShalet, Stephen M
dc.date.accessioned2010-07-27T14:24:10Z
dc.date.available2010-07-27T14:24:10Z
dc.date.issued1991-02
dc.identifier.citationAdult panhypopituitarism presenting as idiopathic growth hormone deficiency in childhood. 1991, 80 (2):255-8 Acta Paediatr Scanden
dc.identifier.issn0001-656X
dc.identifier.pmid2035319
dc.identifier.doi10.1111/j.1651-2227.1991.tb11844.x
dc.identifier.urihttp://hdl.handle.net/10541/108412
dc.description.abstractWe report two patients who presented in childhood with isolated growth hormone deficiency and in whom progressive loss of anterior function led to panhypopituitarism in early adult life. The need for continued follow-up and reassessment of pituitary function in adult life is stressed in the light of the natural history of these patients.
dc.language.isoenen
dc.subject.meshChild
dc.subject.meshFemale
dc.subject.meshFollow-Up Studies
dc.subject.meshGrowth Disorders
dc.subject.meshGrowth Hormone
dc.subject.meshHumans
dc.subject.meshHydrocortisone
dc.subject.meshHypopituitarism
dc.subject.meshMale
dc.subject.meshPituitary Gland, Anterior
dc.subject.meshPituitary Hormones, Anterior
dc.titleAdult panhypopituitarism presenting as idiopathic growth hormone deficiency in childhood.en
dc.typeArticleen
dc.contributor.departmentRoyal Manchester Children's Hospital, UK.en
dc.identifier.journalActa Paediatrica Scandinavicaen
html.description.abstractWe report two patients who presented in childhood with isolated growth hormone deficiency and in whom progressive loss of anterior function led to panhypopituitarism in early adult life. The need for continued follow-up and reassessment of pituitary function in adult life is stressed in the light of the natural history of these patients.


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