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Multiple Pituitary Hormone Deficiency, Empty Sella and Ectopic Neurohypophysis in Turner Syndrome.

AbstractBACKGROUND:
Multiple pituitary hormone deficiency and Turner syndrome have overlapping features in peripubertal girls and is a diagnostic challenge.
CASE CHARACTERISTICS:
16-year-old girl having Turner phenotype undergoing evaluation for severe short stature and pubertal arrest.
OBSERVATION:
45,X karyotype, and multiple pituitary hormone deficiency with empty sella.
INTERVENTION:
Levothyroxine, growth hormone and ethinyl-estradiol replacement resulted in 11 cm height gain with attainment of puberty over 2 years.
MESSAGE:
Patients of Turner syndrome with height <3rd percentile (Turner specific charts) warrant additional pathology evaluation.
AuthorsDeep Dutta, Chitra Selvan, Satinath Mukhopadhyay
JournalIndian pediatrics (Indian Pediatr) Vol. 52 Issue 9 Pg. 803-4 (Sep 2015) ISSN: 0974-7559 [Electronic] India
PMID26519720 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Gonadotropins
  • Growth Hormone
Topics
  • Adolescent
  • Empty Sella Syndrome
  • Female
  • Gonadotropins (deficiency)
  • Growth Hormone (deficiency)
  • Humans
  • Hypothyroidism
  • Turner Syndrome

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