Diagnostic and therapeutic odyssey of two patients with compound heterozygous leptin receptor deficiency.

Zorn, Stefanie; von Schnurbein, Julia; Kohlsdorf, Katja; Denzer, Christian; Wabitsch, Martin

Zorn, Stefanie; von Schnurbein, Julia; Kohlsdorf, Katja; Denzer, Christian; Wabitsch, Martin.

Afiliación

Zorn S; Center for Rare Endocrine Diseases, Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics and Adolescent Medicine, Ulm University Medical Centre, 89075, Ulm, Germany.
von Schnurbein J; Center for Rare Endocrine Diseases, Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics and Adolescent Medicine, Ulm University Medical Centre, 89075, Ulm, Germany.
Kohlsdorf K; Center for Rare Endocrine Diseases, Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics and Adolescent Medicine, Ulm University Medical Centre, 89075, Ulm, Germany.
Denzer C; Center for Rare Endocrine Diseases, Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics and Adolescent Medicine, Ulm University Medical Centre, 89075, Ulm, Germany.
Wabitsch M; Center for Rare Endocrine Diseases, Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics and Adolescent Medicine, Ulm University Medical Centre, 89075, Ulm, Germany. martin.wabitsch@uniklinik-ulm.de.

Mol Cell Pediatr ; 7(1): 15, 2020 Nov 03.

Article en En | MEDLINE | ID: mdl-33140236

Palabras clave

Early-onset obesity; Genetics; Hyperphagia; Leptin receptor; Monogenetic obesity

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Mol Cell Pediatr Año: 2020 Tipo del documento: Article País de afiliación: Alemania

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