id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_gfymbvwtibda5cchl3g5n35yie	Rajesh Joshi	Case Reports	2012.0	2	.pdf	application/pdf	1287	142	57	From the Department of Pediatrics, BJ Wadia Hospital for Children, Parel, Mumbai. Pseudohypoparathyroidism due to deficient end organ response to parathyroid hormone (PTH) is characterized by hypocalcemia, hyperphosphatemia and increased serum PTH. report a case of an 8-year-old girl with pseudohypoparathyroidism without features of Key words: Albright's hereditary osteodystrophy, Hypothyroidism, Parathyroid hormone, PHP without features of AHO who developed Resistance to other hormones (which function via reported rarely [4,5] PHP type 2 does not present with maintain serum calcium levels within the reference range features of AHO, as hypothyroidism develops rarely, as causing hormone resistance. hormones in patients with pseudohypoparathyroidism. We report an 11 year old boy with IgA nephropathy developing chronic myeloid leukemia on and leukemia has been reported rarely in children [2]. Here we report a child with IgA nephropathy developing ratio 0.75), mild renal insufficiency (serum creatinine 1.1 mg/dL), and normal serum albumin and cholesterol.	./cache/work_gfymbvwtibda5cchl3g5n35yie.pdf	./txt/work_gfymbvwtibda5cchl3g5n35yie.txt