Clinical challenges in the management of isolated GH deficiency type IA in adulthood

Summary Isolated GH deficiency type IA (IGHDIA) is an infrequent cause of severe congenital GHD, often managed by pediatric endocrinologists, and hence few cases in adulthood have been reported. Herein, we describe the clinical status of a 56-year-old male with IGHDIA due to a 6.7 kb deletion in GH1...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Endocrinology, diabetes & metabolism case reports diabetes & metabolism case reports, 2014-02, Vol.2014, p.130057-130057
Hauptverfasser:	Casteràs, Anna, Kratzsch, Jürgen, Ferrández, Ángel, Zafón, Carles, Carrascosa, Antonio, Mesa, Jordi
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Anti-GH antibodies Aspirin Bone pain Calcitriol Calcium Cardiology DEXA scan Diabetes mellitus type 2 Empty sella syndrome Genetics Geriatrics Growth hormone deficiency (childhood onset) Growth retardation Haemoglobin A1c HOMA Hypercholesterolaemia Hypovitaminosis D IGF1 IGFBP3 Insight into Disease Pathogenesis or Mechanism of Therapy LDL cholesterol Male Metformin MRI Myalgia Neurology Osteoporosis Paediatrics Pituitary PTH Short stature Spain Total cholesterol Triglycerides Vitamin D White X-ray
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!