Case of hypomagnesemia with secondary hypocalcemia with a novel <i>TRPM6</i> mutation.

Lal, Naresh; Bhardwaj, Swati; Lalgudi Ganesan, Saptharishi; Sharma, Rachna; Jain, Puneet

Case of hypomagnesemia with secondary hypocalcemia with a novel TRPM6 mutation.

Lal, Naresh; Bhardwaj, Swati; Lalgudi Ganesan, Saptharishi; Sharma, Rachna; Jain, Puneet.

Afiliación

Lal N; Pediatric Intensive Care Unit, Department of Pediatrics, BL Kapur Super Specialty Hospital, New Delhi, India.
Bhardwaj S; Division of Pediatric Nephrology, Department of Pediatrics, BL Kapur Super Specialty Hospital, New Delhi, India.
Lalgudi Ganesan S; Department of Critical Care Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
Sharma R; Pediatric Intensive Care Unit, Department of Pediatrics, BL Kapur Super Specialty Hospital, New Delhi, India.
Jain P; Pediatric Intensive Care Unit, Department of Pediatrics, BL Kapur Super Specialty Hospital, New Delhi, India; Epilepsy Program, Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.

Neurol India ; 66(6): 1795-1800, 2018.

Article en En | MEDLINE | ID: mdl-30504582

Asunto(s)

Predisposición Genética a la Enfermedad; Hipocalcemia/genética; Deficiencia de Magnesio/congénito; Mutación/genética; Canales Catiónicos TRPM/genética; Humanos; Hipocalcemia/diagnóstico; Lactante; Magnesio; Deficiencia de Magnesio/diagnóstico; Deficiencia de Magnesio/genética; Masculino

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Canales Catiónicos TRPM / Hipocalcemia / Deficiencia de Magnesio / Mutación Tipo de estudio: Diagnostic_studies Límite: Humans / Infant / Male Idioma: En Revista: Neurol India Año: 2018 Tipo del documento: Article País de afiliación: India

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google