Bartter Syndrome Unveiled: Unraveling the Masquerade of Neuroregression.

Wander, Arvinder; Mahesan, Aakash; Meena, Ankit Kumar; Manikandan, S; Peer, Sameer; Singh, Paramdeep; Gulati, Sheffali

Wander, Arvinder; Mahesan, Aakash; Meena, Ankit Kumar; Manikandan, S; Peer, Sameer; Singh, Paramdeep; Gulati, Sheffali.

Afiliação

Wander A; Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, Bathinda, India.
Mahesan A; Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Meena AK; Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Manikandan S; Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, Bathinda, India.
Peer S; Neuroradiology Division, Department of Radiodiagnosis, All India Institute of Medical Sciences, Bathinda, India.
Singh P; Neuroradiology Division, Department of Radiodiagnosis, All India Institute of Medical Sciences, Bathinda, India.
Gulati S; Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India. sheffaligulati@gmail.com.

Indian J Pediatr ; 91(3): 314, 2024 Mar.

Article em En | MEDLINE | ID: mdl-38114863

Assuntos

Síndrome de Bartter; Humanos; Síndrome de Bartter/diagnóstico; Síndrome de Bartter/genética; Mutação; Diagnóstico Diferencial

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Bartter Limite: Humans Idioma: En Revista: Indian J Pediatr Ano de publicação: 2024 Tipo de documento: Article

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