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Sinus pericranii in achondroplasia: a case report and review of the literature.
Scott, Abbey A; Hodge, Katelyn D; Torres-Martinez, Wilfredo; Dlouhy, Stephen R; Smith, Jodi L; Weaver, David D.
Afiliación
  • Scott AA; aDepartment of Medical and Molecular Genetics bDivision of Pediatric Neurosurgery, Goodman Campbell Brain and Spine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Clin Dysmorphol ; 26(4): 252-255, 2017 Oct.
Article en En | MEDLINE | ID: mdl-28872565
ABSTRACT
In the field of dysmorphology, achondroplasia is a well-known disorder. Sinus pericranii (SP), however, is not. The latter condition is a rare vascular malformation characterized by abnormal connections between the intracranial and the extracranial venous drainage pathways. The etiology of SP remains unclear, and yet, these defects can be present at birth, develop spontaneously later, or evolve following head trauma. Here, we report on a 2-year-old male with achondroplasia, SP, and craniocervical junction stenosis. The latter two defects required surgical correction. SP is an underappreciated malformation that we propose may be induced by increased intracranial pressure. This case appears to be the first report of this condition in achondroplasia.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Acondroplasia / Seno Pericraneal Límite: Child, preschool / Humans / Infant / Male Idioma: En Revista: Clin Dysmorphol Asunto de la revista: TERATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Acondroplasia / Seno Pericraneal Límite: Child, preschool / Humans / Infant / Male Idioma: En Revista: Clin Dysmorphol Asunto de la revista: TERATOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos