Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases

ERDÖL Ş., SAĞLAM H.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.8, sa.3, ss.330-333, 2016 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 8 Sayı: 3
  • Basım Tarihi: 2016
  • Doi Numarası: 10.4274/jcrpe.2288
  • Dergi Adı: JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.330-333
  • Anahtar Kelimeler: Inherited, metabolic diseases, endocrine dysfunction, children, MITOCHONDRIAL-DNA DELETION, KEARNS-SAYRE-SYNDROME, DIABETES-MELLITUS, ADRENAL INSUFFICIENCY, CHILD, ACERULOPLASMINEMIA, IDENTIFICATION
  • Bursa Uludağ Üniversitesi Adresli: Evet

Özet

Objective: Inherited metabolic diseases (IMDs) can affect many organ systems, including the endocrine system. There are limited data regarding endocrine dysfunctions related to IMDs in adults, however, no data exist in pediatric patients with IMDs. The aim of this study was to investigate endocrine dysfunctions in patients with IMDs by assessing their demographic, clinical, and laboratory data.