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Hypopituitarism masquerading as Prasad's syndrome: A case report

  • Fatma Demirel
  • , Tekin Aksu
  • , Ihsan Esen
  • , Neşe Yarali
  • , Gülhan Karakaya
  • , Bahattin Tunç
  • Ankara Children’s Hematology and Oncology Training Hospital

Araştırma çıktısı: Dergiye katkıMakaleHakemli

1 Alıntı (Scopus)

Özet

Prasad's syndrome is characterized by geophagia, growth retardation, hypogonadism, and zinc deficiency. We report a 15-year-old boy whose medical history and clinical and laboratory findings were fully compatible with Prasad's syndrome. In addition to severe growth retardation and pubertal delay, iron deficiency anemia and zinc deficiency were determined. His gliadin and endomysium antibodies were negative. The thyroid hormone levels were in normal range but basal gonadotropins and testosterone levels were low for his age. Detailed endocrinological evaluation revealed growth hormone deficiency and hypogonadotropic hypogonadism. Pituitary gland magnetic resonance imaging revealed pituitary hypoplasia. In our opinion, before the diagnosis of Prasad's syndrome, endocrine evaluation should be done in these patients and hypopituitarism should be ruled out. Hypogonadotropic hypogonadism and growth hormone deficiency may be masked by Prasad's syndrome.

Orijinal dilİngilizce
Sayfa (başlangıç-bitiş)702-704
Sayfa sayısı3
DergiTurkish Journal of Pediatrics
Hacim53
Basın numarası6
Yayın durumuYayınlandı - 2011
Harici olarak yayınlandıEvet

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