Abnormal pubertal development in primary hypothyroidism.

Abstract:

:We have studied three patients (1M, 2F), age range 10.9 to 15.5 years, who had abnormal sexual maturation secondary to primary hypothyroidism. The boy had inappropriately large testes for his stage of puberty, the girls had isolated breast development and there was absence of pubertal growth acceleration. FSH, LH, TSH and GH secretion, pituitary imaging and ovarian ultrasound morphology were studied before and during thyroxine treatment. In the hypothyroid state, FSH levels were elevated with abnormal pulsatility and LH:FSH concentrations were reversed.

journal_name

Clin Endocrinol (Oxf)

journal_title

Clinical endocrinology

authors

Pringle PJ,Stanhope R,Hindmarsh P,Brook CG

doi

10.1111/j.1365-2265.1988.tb03682.x

subject

Has Abstract

pub_date

1988-05-01 00:00:00

pages

479-86

issue

5

eissn

0300-0664

issn

1365-2265

journal_volume

28

pub_type

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