White matter abnormality in Jacobsen syndrome assessed by serial MRI.

Fujino, Shuhei; Yoshihashi, Hiroshi; Takeda, Ryojun; Ihara, Satoshi; Miyama, Sahoko

Fujino, Shuhei; Yoshihashi, Hiroshi; Takeda, Ryojun; Ihara, Satoshi; Miyama, Sahoko.

Afiliación

Fujino S; Department of Neurology, Tokyo Metropolitan Children's Medical Center, Japan. Electronic address: n_r_h_c_1616@yahoo.co.jp.
Yoshihashi H; Department of Medical Genetics, Tokyo Metropolitan Children's Medical Center, Japan.
Takeda R; Department of Medical Genetics, Tokyo Metropolitan Children's Medical Center, Japan.
Ihara S; Department of Neurosurgery, Tokyo Metropolitan Children's Medical Center, Japan.
Miyama S; Department of Neurology, Tokyo Metropolitan Children's Medical Center, Japan.

Brain Dev ; 42(8): 621-625, 2020 Sep.

Article en En | MEDLINE | ID: mdl-32507665

Asunto(s)

Síndrome de Deleción Distal 11q de Jacobsen/diagnóstico por imagen; Síndrome de Deleción Distal 11q de Jacobsen/genética; Sustancia Blanca/anomalías; Sustancia Blanca/diagnóstico por imagen; Anomalías Craneofaciales; Discapacidades del Desarrollo; Femenino; Humanos; Lactante; Imagen por Resonancia Magnética; Hipotonía Muscular

Palabras clave

Cerebral white matter abnormality; Hepatic and glial cell adhesion molecules (HEPACAM/GlialCAM); Jacobsen syndrome; Megalencephalic leukoencephalopathy with subcortical cysts type 2B (MLC2B)

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Deleción Distal 11q de Jacobsen / Sustancia Blanca Límite: Female / Humans / Infant Idioma: En Revista: Brain Dev Año: 2020 Tipo del documento: Article

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