{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["10"],"submitter":["Elli FM"],"funding":["Ministero della Salute"],"pubmed_abstract":["Pseudohypoparathyroidism (PHP) is a rare endocrine disorder derived from the defective activation of the cAMP pathway by the parathyroid hormone secondary to GNAS molecular defects. PHP subtypes are defined by the presence/absence of specific clinical/biochemical features. PHP1A is characterized by resistance to multiple hormones with features of Albright hereditary osteodystrophy (AHO), while pseudopseudohypoparathyroidism (PPHP) is characterized by AHO in the absence of PTH resistance. Small subsets of PHP and PPHP patients without known molecular defects have been re-diagnosed as being affected by the brachydactyly-mental retardation syndrome (BDMR), also known as the AHO-like syndrome. This study aimed to analyse 24 PHP1A and 51 PPHP patients without a molecular diagnosis for the prese"],"journal":["Frontiers in endocrinology"],"pagination":["604"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6727065"],"repository":["biostudies-literature"],"pubmed_title":["2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance."],"pmcid":["PMC6727065"],"pubmed_authors":["Bordogna P","Mantovani G","Maffini MA","Elli FM","de Sanctis L","Madeo B","Arosio M","Pirelli A"],"additional_accession":[]},"is_claimable":false,"name":"2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance.","description":"Pseudohypoparathyroidism (PHP) is a rare endocrine disorder derived from the defective activation of the cAMP pathway by the parathyroid hormone secondary to GNAS molecular defects. PHP subtypes are defined by the presence/absence of specific clinical/biochemical features. PHP1A is characterized by resistance to multiple hormones with features of Albright hereditary osteodystrophy (AHO), while pseudopseudohypoparathyroidism (PPHP) is characterized by AHO in the absence of PTH resistance. Small subsets of PHP and PPHP patients without known molecular defects have been re-diagnosed as being affected by the brachydactyly-mental retardation syndrome (BDMR), also known as the AHO-like syndrome. This study aimed to analyse 24 PHP1A and 51 PPHP patients without a molecular diagnosis for the prese","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019","modification":"2026-04-13T03:20:58.09Z","creation":"2019-10-11T07:03:39Z"},"accession":"S-EPMC6727065","cross_references":{"pubmed":["31555217"],"doi":["10.3389/fendo.2019.00604"]}}