Myhre syndrome (MS) (MIM 139210) is a rare disorder characterized by short stature, mental retardation, muscular build, blepharophimosis, and decreased joint mobility. We report on a 14-year-old boy with clinical findings consistent with a diagnosis of Myhre syndrome, associated with autism and peculiar skin histological findings.

Case of Myhre syndrome with autism and peculiar skin histological findings / Titomanlio, L; Marzano, Mg; Rossi, E; D'Armiento, Maria; De Brasi, D; Vega, Gr; Andreucci, Mv; Orsini, Av; Santoro, L; Sebastio, Gianfranco. - In: AMERICAN JOURNAL OF MEDICAL GENETICS. - ISSN 0148-7299. - STAMPA. - 103:(2001), pp. 163-165.

Case of Myhre syndrome with autism and peculiar skin histological findings.

D'ARMIENTO, MARIA;SEBASTIO, GIANFRANCO
2001

Abstract

Myhre syndrome (MS) (MIM 139210) is a rare disorder characterized by short stature, mental retardation, muscular build, blepharophimosis, and decreased joint mobility. We report on a 14-year-old boy with clinical findings consistent with a diagnosis of Myhre syndrome, associated with autism and peculiar skin histological findings.
2001
Case of Myhre syndrome with autism and peculiar skin histological findings / Titomanlio, L; Marzano, Mg; Rossi, E; D'Armiento, Maria; De Brasi, D; Vega, Gr; Andreucci, Mv; Orsini, Av; Santoro, L; Sebastio, Gianfranco. - In: AMERICAN JOURNAL OF MEDICAL GENETICS. - ISSN 0148-7299. - STAMPA. - 103:(2001), pp. 163-165.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/516958
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