1.
Article
in English
| IMSEAR
| ID: sea-149737
2.
Article
in English
| IMSEAR
| ID: sea-149829
3.
Indian Pediatr
;
2012 August; 49(8): 667-668
Article
in English
| IMSEAR
| ID: sea-169432
ABSTRACT
Pseudohypoparathyroidism due to deficient end organ response to parathyroid hormone (PTH) is characterized by hypocalcemia, hyperphosphatemia and increased serum PTH. We report a case of an 8-year-old girl with pseudohypoparathyroidism without features of Albright’s hereditary osteodystrophy. The case is of interest as the child on serial follow-up over a period of 2 years developed hypothyroidism. This is a rare feature seen in pseudohypoparathyroidism type1b.