Novel homozygous leptin receptor mutation in an infant with monogenic obesity.

Boro, Hiya; Bundela, Vikash; Mannar, Velmurugan; Nagendra, Lakshmi; Jain, Vinita; Jain, Bimal; Kumar, Senthil; Agstam, Sourabh

Boro, Hiya; Bundela, Vikash; Mannar, Velmurugan; Nagendra, Lakshmi; Jain, Vinita; Jain, Bimal; Kumar, Senthil; Agstam, Sourabh.

Afiliação

Boro H; Endocrinology and Metabolism, Aadhar Health Institute, India.
Bundela V; Gastroenterology, Aadhar Health Institute, India.
Mannar V; Endocrinology, Aarupadai Veedu Medical College, India.
Nagendra L; Endocrinology, JSS Medical College, India.
Jain V; Pediatrics, Aadhar Health Institute, India.
Jain B; Scientific Affairs Team, MedGenome Laboratory, IndiaScientific Affairs Team, MedGenome Laboratory, India.
Kumar S; Scientific Affairs Team, MedGenome Laboratory, India.
Agstam S; Cardiology, Vardhman Mahavir Medical College and Safdarjung Hospital, India.

Pediatr Endocrinol Diabetes Metab ; 29(2): 118-123, 2023.

Article em En | MEDLINE | ID: mdl-37728464

Assuntos

Leptina; Receptores para Leptina; Lactente; Masculino; Humanos; Leptina/genética; Receptores para Leptina/genética; Hiperfagia; Éxons; Obesidade/genética

Palavras-chave

leptin; leptin receptor; monogenic obesity.; setmelanotide; splice site mutation

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leptina / Receptores para Leptina Tipo de estudo: Prognostic_studies Limite: Humans / Infant / Male Idioma: En Revista: Pediatr Endocrinol Diabetes Metab Assunto da revista: ENDOCRINOLOGIA / METABOLISMO / PEDIATRIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Índia

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