Pseudohypoparathyroidism-Albright hereditary osteodystrophy.
dc.contributor.author | Rastogi, S | en_US |
dc.contributor.author | Gupta, S | en_US |
dc.contributor.author | Misra, P K | en_US |
dc.contributor.author | Rastogi, D | en_US |
dc.date.accessioned | 1998-05-20 | en_US |
dc.date.accessioned | 2009-05-30T15:25:09Z | |
dc.date.available | 1998-05-20 | en_US |
dc.date.available | 2009-05-30T15:25:09Z | |
dc.date.issued | 1998-05-20 | en_US |
dc.description.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. | en_US |
dc.description.affiliation | Department of Pediatrics, King George's Medical College, Lucknow, India. | en_US |
dc.identifier.citation | Rastogi S, Gupta S, Misra PK, Rastogi D. Pseudohypoparathyroidism-Albright hereditary osteodystrophy. Indian Journal of Pediatrics. 1998 May-Jun; 65(3): 477-80 | en_US |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/83603 | |
dc.language.iso | eng | en_US |
dc.source.uri | https://medind.nic.in/icb/icbai.shtml | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Basal Ganglia Diseases --diagnosis | en_US |
dc.subject.mesh | Calcinosis --diagnosis | en_US |
dc.subject.mesh | Diagnosis, Differential | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Fibrous Dysplasia, Polyostotic --diagnosis | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Pseudohypoparathyroidism --diagnosis | en_US |
dc.subject.mesh | Tomography, X-Ray Computed | en_US |
dc.title | Pseudohypoparathyroidism-Albright hereditary osteodystrophy. | en_US |
dc.type | Case Reports | en_US |
dc.type | Journal Article | en_US |
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