Literature DB >> 33451138

Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis.

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

Mesh:

Substances:

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


  27 in total

Review 1.  An additional patient with a homozygous mutation in DCPS contributes to the delination of Al-Raqad syndrome.

Authors:  Viola Alesi; Rossella Capolino; Silvia Genovesea; Teresa Capriati; Sara Loddo; Giusy Calvieri; Chiara Calacci; Andrea Diociaiuti; Antonella Diamanti; Antonio Novelli; Bruno Dallapiccola
Journal:  Am J Med Genet A       Date:  2018-10-05       Impact factor: 2.802

2.  Type I procollagen C-propeptide defects: study of genotype-phenotype correlation and predictive role of crystal structure.

Authors:  Sofie Symoens; David J S Hulmes; Jean-Marie Bourhis; Paul J Coucke; Anne De Paepe; Fransiska Malfait
Journal:  Hum Mutat       Date:  2014-10-18       Impact factor: 4.878

3.  HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype.

Authors:  Qing Fang; Anna Flavia Figueredo Benedetti; Qianyi Ma; Louise Gregory; Jun Z Li; Mehul Dattani; Abdollah Sadeghi-Nejad; Ivo J P Arnhold; Berenice Bilharinho Mendonca; Sally A Camper; Luciani R Carvalho
Journal:  Clin Endocrinol (Oxf)       Date:  2016-04-28       Impact factor: 3.478

4.  Autosomal Recessive Osteogenesis Imperfecta Caused by a Novel Homozygous COL1A2 Mutation.

Authors:  Alice Costantini; Symeon Tournis; Anders Kämpe; Noor Ul Ain; Fulya Taylan; Artemis Doulgeraki; Outi Mäkitie
Journal:  Calcif Tissue Int       Date:  2018-03-23       Impact factor: 4.333

5.  Homozygosity by descent for a COL1A2 mutation in two sibs with severe osteogenesis imperfecta and mild clinical expression in the heterozygotes.

Authors:  A De Paepe; L Nuytinck; M Raes; J P Fryns
Journal:  Hum Genet       Date:  1997-04       Impact factor: 4.132

6.  Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.

Authors:  R Harripaul; N Vasli; A Mikhailov; M A Rafiq; K Mittal; C Windpassinger; T I Sheikh; A Noor; H Mahmood; S Downey; M Johnson; K Vleuten; L Bell; M Ilyas; F S Khan; V Khan; M Moradi; M Ayaz; F Naeem; A Heidari; I Ahmed; S Ghadami; Z Agha; S Zeinali; R Qamar; H Mozhdehipanah; P John; A Mir; M Ansar; L French; M Ayub; J B Vincent
Journal:  Mol Psychiatry       Date:  2017-04-11       Impact factor: 15.992

7.  Enhanced repression by HESX1 as a cause of hypopituitarism and septooptic dysplasia.

Authors:  Ronald N Cohen; Laurie E Cohen; Diego Botero; Christine Yu; Angela Sagar; Magdalena Jurkiewicz; Sally Radovick
Journal:  J Clin Endocrinol Metab       Date:  2003-10       Impact factor: 5.958

8.  Serine for glycine substitutions in type I collagen in two cases of type IV osteogenesis imperfecta (OI). Additional evidence for a regional model of OI pathophysiology.

Authors:  J C Marini; M B Lewis; Q Wang; K J Chen; B M Orrison
Journal:  J Biol Chem       Date:  1993-02-05       Impact factor: 5.157

9.  Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locus.

Authors:  L D Spotila; L Sereda; D J Prockop
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

10.  The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfecta.

Authors:  A C Nicholls; G Osse; H G Schloon; H G Lenard; S Deak; J C Myers; D J Prockop; W R Weigel; P Fryer; F M Pope
Journal:  J Med Genet       Date:  1984-08       Impact factor: 6.318

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  1 in total

1.  Molecular Research in Medical Genetics.

Authors:  Emanuela Viggiano
Journal:  Int J Mol Sci       Date:  2022-06-14       Impact factor: 6.208

  1 in total

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