A case of Friedreich ataxia in an adolescent with 16p11.2 microdeletion syndrome.

Pelliccia, Valentina; Ferranti, Silvia; Mostardini, Rosa; Grosso, Salvatore

Pelliccia, Valentina; Ferranti, Silvia; Mostardini, Rosa; Grosso, Salvatore.

Affiliation

Pelliccia V; Dipartimento di Medicina Molecolare e dello Sviluppo, Universita' degli Studi di Siena, viale Bracci, 53100, Siena, Italy.
Ferranti S; Dipartimento di Medicina Molecolare e dello Sviluppo, Universita' degli Studi di Siena, viale Bracci, 53100, Siena, Italy. silvia.ferranti@hotmail.it.
Mostardini R; U.O.C. Pediatria, Azienda Ospedaliera Universitaria Senese, viale Bracci 16, 53100, Siena, Italy.
Grosso S; Dipartimento di Medicina Molecolare e dello Sviluppo, Universita' degli Studi di Siena, viale Bracci, 53100, Siena, Italy.

Neurol Sci ; 41(3): 721-722, 2020 03.

Article in En | MEDLINE | ID: mdl-31578651

Subject(s)

Autistic Disorder/diagnosis; Chromosome Disorders/diagnosis; Developmental Disabilities/diagnosis; Friedreich Ataxia/diagnosis; Intellectual Disability/diagnosis; Adolescent; Autistic Disorder/complications; Chromosome Deletion; Chromosome Disorders/complications; Chromosomes, Human, Pair 16; Developmental Disabilities/etiology; Friedreich Ataxia/etiology; Humans; Intellectual Disability/complications; Male

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Full text: 1 Database: MEDLINE Main subject: Autistic Disorder / Friedreich Ataxia / Developmental Disabilities / Chromosome Disorders / Intellectual Disability Type of study: Etiology_studies Limits: Adolescent / Humans / Male Language: En Journal: Neurol Sci Journal subject: NEUROLOGIA Year: 2020 Type: Article Affiliation country: Italy

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