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Endocrine Abstracts (2019) 63 P115 | DOI: 10.1530/endoabs.63.P115

ECE2019 Poster Presentations Calcium and Bone 1 (60 abstracts)

Severe diffuse tissue calcifications in a patient with pseudohypoparathyroidism type 1 A due to a novel large deletion of GNAS gene

Alessandro Brancatella 1 , Giovanna Mantovani 2 , Claudio Marcocci 1 & Filomena Cetani 1

1Department of Clinical and Experimental Medicine, Endocrine Unit, University of Pisa, Pisa, Italy; 2Endocrinology Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, and Department of Clinical Sciences and Community Health, University of Milan, Milano, Italy.

Pseudohypoparathyroidism type 1 A (PHP-1A) is a rare genetic disorder characterized by hypocalcemia, hyperphosfatemia, multi hormones resistance (PTH, TSH, Calcitonin, GH) associated with Albright hereditary osteodystrophy (AHO) features. The disease is caused by GNAS haploinsufficiency due to inherited inactivating mutation of GNAS-gene that codes for the stimulatory alfa subunit of G protein. A positive genotype-phenotype correlation was recently hypothesized. The purpose of this work is to describe a new family affected by PHP-1A. The proband, a 18 years old man, came for the first time to our attention in 2017 for hypocalcemia diagnosed after a tetanic crisis. Physical examination showed the typical features of AHO: round face, stocky habitus with short stature, brachydactyly and ectopic-severe ossification in the back and in the legs. Laboratory tests showed low levels of calcium, high levels of phosphate and high levels of PTH, TSH and calcitonin despite therapy with calcium carbonate, calcitriol and levothyroxine. Computed tomography showed diffuse calcifications ‘rosary-like’ in the cortex and scalp. Bone radiography showed diffuse soft tissue and costal cartilage calcifications and marked brachydactyly and brachimetacarpy. Family history was remarkable for hypocalcemic crisis associated with neurocognitive impairment and cerebral calcification in the brother. The genetic analysis of the GNAS gene showed a novel large deletion (encompassing exons 1–7), in the proband, in the brother and in the mother. The daily dose of calcitriol, calcium carbonate and L-thyroxine was increased with good control of hypocalcemia thereafter. At the latest evaluation, serum calcium and TSH levels were normal with a reduction of PTH levels. In conclusion, we have identified an additional PHP-1A family with severe phenotype that supports the hypothesis of a positive genotype-phenotype correlation.

Volume 63

21st European Congress of Endocrinology

Lyon, France
18 May 2019 - 21 May 2019

European Society of Endocrinology 

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