Literature DB >> 11338227

Pseudohypoparathyroidism in a mother and son: phenotypic variability and associated disorder.

M Ray1, J Goraya, S Basu, S Mitra, B Poddar, V Parmar.   

Abstract

A 2-month-old infant with clinical features of hypothyroidism presented with hypocalcemic seizures. The maternal phenotypic features aroused the suspicion of pseudohypoparathyroidism which was confirmed in both by biochemical and endocrinological investigations. Though the child had clinical and radiological features to suggest hypothyroidism he had normal free thyroxine and only slightly elevated thyroid stimulating hormone levels. Special note is made of the intra and interpatient variability of this rare inherited disorder.

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Year:  2001        PMID: 11338227     DOI: 10.1007/BF02723206

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  14 in total

1.  Pseudohypoparathyroidism-Albright hereditary osteodystrophy.

Authors:  S Rastogi; S Gupta; P K Misra; D Rastogi
Journal:  Indian J Pediatr       Date:  1998 May-Jun       Impact factor: 1.967

2.  Skeletal abnormalities, hypocalcaemia and intracranial calcification.

Authors:  R Khot; M Paithankar; H R Salkar; V L Gupta; A Satav
Journal:  Postgrad Med J       Date:  1998-02       Impact factor: 2.401

3.  [Primary hypothyroidism revealing pseudohypoparathyroidism without hypocalcemia and hyperphosphoremia].

Authors:  R Coutant; J C Carel; L Mathivon; C Boisson Lesage; D Renier; M Garabédian; J L Chaussain
Journal:  Arch Pediatr       Date:  1997-05       Impact factor: 1.180

4.  Pseudohypoparathyroidism type 1a presenting as congenital hypothyroidism.

Authors:  Y Weisman; A Golander; Z Spirer; Z Farfel
Journal:  J Pediatr       Date:  1985-09       Impact factor: 4.406

5.  Probable autosomal recessive inheritance in a family with Albright's hereditary osteodystrophy and an evaluation of the genetics of the disorder.

Authors:  S D Cederbaum; B M Lippe
Journal:  Am J Hum Genet       Date:  1973-11       Impact factor: 11.025

6.  Infantile hypothyroidism in two sibs: an unusual presentation of pseudohypoparathyroidism type Ia.

Authors:  M A Levine; T S Jap; W Hung
Journal:  J Pediatr       Date:  1985-12       Impact factor: 4.406

7.  Resistance to multiple hormones in patients with pseudohypoparathyroidism. Association with deficient activity of guanine nucleotide regulatory protein.

Authors:  M A Levine; R W Downs; A M Moses; N A Breslau; S J Marx; R D Lasker; R E Rizzoli; G D Aurbach; A M Spiegel
Journal:  Am J Med       Date:  1983-04       Impact factor: 4.965

8.  Multiple associated endocrine abnormalities in a patient with pseudohypoparathyroidism type 1a.

Authors:  M Shima; O Nose; K Shimizu; Y Seino; H Yabuuchi; T Saito
Journal:  Eur J Pediatr       Date:  1988-06       Impact factor: 3.183

9.  Pseudohypoparathyroidism: defective excretion of 3',5'-AMP in response to parathyroid hormone.

Authors:  L R Chase; G L Melson; G D Aurbach
Journal:  J Clin Invest       Date:  1969-10       Impact factor: 14.808

10.  Defect of receptor-cyclase coupling protein in psudohypoparathyroidism.

Authors:  Z Farfel; A S Brickman; H R Kaslow; V M Brothers; H R Bourne
Journal:  N Engl J Med       Date:  1980-07-31       Impact factor: 91.245

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