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Clin Dysmorphol ; 29(3): 123-126, 2020 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-32282352

RESUMEN

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.


Asunto(s)
Pie Equinovaro/genética , Hidroxiprostaglandina Deshidrogenasas/genética , Osteoartropatía Hipertrófica Primaria/genética , Adulto , Pueblo Asiatico , Niño , Preescolar , Pie Equinovaro/fisiopatología , Familia , Femenino , Humanos , Hidroxiprostaglandina Deshidrogenasas/metabolismo , India , Masculino , Mutación/genética , Mutación Missense/genética , Osteoartropatía Hipertrófica Primaria/fisiopatología , Linaje
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