Pseudohypoparathyroidism-Albright Hereditary Osteodystrophy

Shantanu Rastogi, Sanjay Gupta, P. K. Misra, Deepa Rastogi

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

A 13 year old girl with short stature, and retarded mental growth with coarse facies and deranged thyroid function test was initially suspected as a case of hypothyroidism and was started on thyroxine. Lack of response to treatment and on further investigations it was diagnosed as a case of pseudohypoparathyroidism. High index of suspicion and careful evaluation is important to diagnose such an entity.

Original languageEnglish (US)
Pages (from-to)477-480
Number of pages4
JournalIndian Journal of Pediatrics
Volume65
Issue number3
StatePublished - May 1998
Externally publishedYes

Fingerprint

Pseudohypoparathyroidism
Thyroid Function Tests
Hypothyroidism
Thyroxine
Growth
Therapeutics
Albright's hereditary osteodystrophy

Keywords

  • Albright
  • Pseudohypoparathyroid

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Pseudohypoparathyroidism-Albright Hereditary Osteodystrophy. / Rastogi, Shantanu; Gupta, Sanjay; Misra, P. K.; Rastogi, Deepa.

In: Indian Journal of Pediatrics, Vol. 65, No. 3, 05.1998, p. 477-480.

Research output: Contribution to journalArticle

Rastogi, S, Gupta, S, Misra, PK & Rastogi, D 1998, 'Pseudohypoparathyroidism-Albright Hereditary Osteodystrophy', Indian Journal of Pediatrics, vol. 65, no. 3, pp. 477-480.
Rastogi, Shantanu ; Gupta, Sanjay ; Misra, P. K. ; Rastogi, Deepa. / Pseudohypoparathyroidism-Albright Hereditary Osteodystrophy. In: Indian Journal of Pediatrics. 1998 ; Vol. 65, No. 3. pp. 477-480.
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