Hypoparathyroidism and late-onset hypogonadism in an adult male with familial 22q11.2 deletion syndrome: a case report with 3-year follow-up and review of the literature.

Chen, Xuelian; Yang, Lichuan; Li, Jianwei; Tan, Huiwen

Chen, Xuelian; Yang, Lichuan; Li, Jianwei; Tan, Huiwen.

Afiliación

Chen X; Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Yang L; Department of Nephrology, West China Hospital of Sichuan University, Chengdu, 610041, Sichuan, China.
Li J; Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Tan H; Department of Nephrology, West China Hospital of Sichuan University, Chengdu, 610041, Sichuan, China.

BMC Endocr Disord ; 22(1): 278, 2022 Nov 12.

Article en En | MEDLINE | ID: mdl-36371175

Asunto(s)

Síndrome de DiGeorge; Hipogonadismo; Hipoparatiroidismo; Masculino; Humanos; Síndrome de DiGeorge/complicaciones; Síndrome de DiGeorge/diagnóstico; Síndrome de DiGeorge/genética; Estudios de Seguimiento; Hipoparatiroidismo/complicaciones; Fenotipo; Hipogonadismo/complicaciones

Palabras clave

22q11.2DS; Case report; Chronic kidney disease; DiGeorge syndrome; Hypocalcemia; Hypogonadism; Hypoparathyroidism; Metabolic syndrome

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de DiGeorge / Hipogonadismo / Hipoparatiroidismo Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Male Idioma: En Revista: BMC Endocr Disord Año: 2022 Tipo del documento: Article País de afiliación: China

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