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Clin Dysmorphol ; 29(3): 123-126, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32282352

ABSTRACT

15-Hydroxyprostaglandin dehydrogenase is NAD-dependent catalytic enzyme involved in prostaglandin biosynthesis pathway encoded by HPGD. The pathogenic variations in HPGD cause primary hypertrophic osteoarthropathy (PHO). The objective of the present study is to identify the genetic basis in patients with digital clubbing due to PHO. We performed detailed clinical and radiographic evaluation and exome sequencing in patients from three unrelated Indian families with PHO. Exome sequencing revealed two novel, c.34G>A (p.Gly12Ser) and c.313C>T (p.Gln105*) and a known variant, c.418G>C (p.Ala140Pro) in HPGD. Herein, we add three Indian families to HPGD mutation spectrum and review the literature on variants in this gene.


Subject(s)
Clubfoot/genetics , Hydroxyprostaglandin Dehydrogenases/genetics , Osteoarthropathy, Primary Hypertrophic/genetics , Adult , Asian People , Child , Child, Preschool , Clubfoot/physiopathology , Family , Female , Humans , Hydroxyprostaglandin Dehydrogenases/metabolism , India , Male , Mutation/genetics , Mutation, Missense/genetics , Osteoarthropathy, Primary Hypertrophic/physiopathology , Pedigree
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