| Literature DB >> 33451138 |
Viola Alesi1, Maria Lisa Dentici2, Silvia Genovese1, Sara Loddo1, Emanuele Bellacchio3, Valeria Orlando1, Silvia Di Tommaso1, Giorgia Catino1, Chiara Calacci1, Giusy Calvieri1, Daniele Pompili1, Graziamaria Ubertini4, Bruno Dallapiccola2, Rossella Capolino2, Antonio Novelli1.
Abstract
We report on a patient born to consanguineous parents, presenting with Growth Hormone Deficiency (GHD) and osteoporosis. SNP-array analysis and exome sequencing disclosed long contiguous stretches of homozygosity and two distinct homozygous variants in HESX1 (Q6H) and COL1A1 (E1361K) genes. The HESX1 variant was described as causative in a few subjects with an incompletely penetrant dominant form of combined pituitary hormone deficiency (CPHD). The COL1A1 variant is rare, and so far it has never been found in a homozygous form. Segregation analysis showed that both variants were inherited from heterozygous unaffected parents. Present results further elucidate the inheritance pattern of HESX1 variants and recommend assessing the clinical impact of variants located in C-terminal propeptide of COL1A1 gene for their potential association with rare recessive and early onset forms of osteoporosis.Entities:
Keywords: COL1A1; CPHD; E1361K; HESX1; Q6H; combined pituitary hormone deficiency; osteoporosis
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Year: 2021 PMID: 33451138 PMCID: PMC7828579 DOI: 10.3390/ijms22020750
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923