Results 71 to 80 of about 2,981 (206)
Pseudo-pseudohypoparathyroidism. A disputable syndrome
Two cases of the so-called syndrome of pseudo-pseudohypoparathyroidism are described. Metacarpal and metatarsal defects may be seen not only in pseudo-pseudohypoparathyroidism, but are occasionally encountered in patients with multiple congenital defects.
Alivisatos, J.G., Papadatos, C.
core
Hyperphosphatemia in Celiac Disease: Hereditary or Acquired Pseudohypoparathyroidism
Calcium and vitamin D deficiencies caused by intestinal malabsorption in celiac disease lead to severe impairments of calcium and bone metabolisms. Indeed, malabsorption of calcium results in secondary hyperparathyroidism.
Ramazan Gen +2 more
doaj +2 more sources
Pseudohypoparathyroidism– A Clinical Rarity
Pseudohypoparathyroidism is a metabolic disease caused by an inability of the body to respond appropriately to parathyroid hormone (PTH), the principal hormone that regulates calcium and phosphorous levels in the body.
Bipa Mazumdar +3 more
core
A Case of Pseudohypoparathyroidism without Albright's Hereditary Osteodystrophy in an Adult [PDF]
Pseudohypoparathyroidism is a rare disease caused by resistance to parathyroid hormone, and is associated with typical clinical typical symptoms such as tetany and seizures, hypocalcemia, hyperphosphatemia and increased parathyroid hormone levels ...
박종숙 +6 more
core +1 more source
Regulation of 1,25 (OH)2D synthesis in hypoparathyroidism and pseudohypoparathyroidism
We examined the regulation of 1,25-dihydroxyvitamin D [1,25(OH)2D] synthesis in patients with hypoparathyroidism (n = 5) and pseudohypoparathyroidism (n = 5) by administration of parathyroid extract (PTE) and N6,O2-dibutyryladenosine 3',5'-cyclic ...
N. A. Breslau, R. S. Weinstock
core +1 more source
Albright hereditary osteodystrophy: A rare case report
Albright hereditary osteodystrophy (AHO) is a rare hereditary metabolic disorder that may be associated with or without resistant to parathyroid hormone (pseudohypoparathyroidism).
Goswami M +4 more
doaj
A 13 year old Asian girl presenting with apparent hysterical paralysis and subsequent rapid cycling bipolar mood disorder was found to have biochemical evidence of pseudohypoparathyroidism type II.
Prendergast, M +5 more
core +1 more source
Management of pseudohypoparathyroidism
Purpose of review This review is timely given the 2018 publication of the first international Consensus Statement for the diagnosis and management of pseudohypoparathyroidism (PHP) and related disorders. The purpose of this review is to provide the knowledge needed to recognize and manage PHP1A, pseudopseudohypoparathyroidism ...
openaire +3 more sources
Abnormalities in Erythrocyte Membrane Protein in Pseudohypoparathyroidism Type l1) [PDF]
Summary: The erythrocyte membrane proteins of patients with pseudohypoparathyroidism type l and healthy volunteers were analysed by two-dimensional polyacrylamide gel electrophoresis in combination with a sensitive silver staining method ...
Matsumoto, Akira +3 more
core +1 more source
Supplemental information for the manuscript entitled "Neonatal and early infancy features of patients with inactivating PTH/PTHrP Signaling Disorders ...
Del Sindaco, Giulia
core +1 more source

