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Clinical and histopathological features of conjunctival "Teddy bear" granuloma: A case series.

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[Dandy-Walker variant: Case report].

José E Cueva-Núñez1, Alejandra Lozano-Bustillo1, Merlyn S Irias-Álvarez1

  • 1Medicina General, Facultad de Ciencias Médicas, Universidad Nacional Autónoma de Honduras, Tegucigalpa, Honduras.

Revista Chilena De Pediatria
|March 16, 2016
PubMed
Summary
This summary is machine-generated.

Dandy Walker variant, a rare condition, may not cause symptoms and can be linked to other genetic disorders. Multidisciplinary management is key for this cerebellar malformation.

Keywords:
Complejo Dandy WalkerDandy Walker complexDandy-Walker variantHipoplasia cerebelosa parcialHipoplasia de vermis aisladaIsolated vermian hypoplasiaPartial cerebellar hypoplasiaVariante de Dandy Walker

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Area of Science:

  • Neuroscience
  • Developmental Biology
  • Medical Genetics

Background:

  • Dandy Walker variant is characterized by cerebellar vermis hypoplasia and potential posterior fossa abnormalities.
  • It is crucial to understand the causes of prenatal malformations and their comprehensive management.

Observation:

  • A case study of an 8-year-old male with a history of Infantile Cerebral Palsy and epilepsy presented with seizures and psychomotor developmental delay.
  • Neuroimaging revealed communication between the cisterna magna and an enlarged fourth ventricle, with partial cerebellar vermis hypoplasia.

Findings:

  • The observed neuroimaging findings were consistent with a Dandy Walker variant diagnosis.
  • This condition can be asymptomatic, and imaging may not always correlate with developmental disorders due to associated syndromes or chromosomal abnormalities.

Implications:

  • The clinical presentation and prognosis of Dandy Walker variant are influenced by associated conditions.
  • A multidisciplinary approach is essential for managing Dandy Walker variant, with treatment tailored to individual symptoms.