Article
A unique case of progressive hemifacial microsomia or Parry-Romberg syndrome associated with limb and brain anomalies with normal neurological findings: A review of the literature.
European journal of medical genetics - 1 Sept 2021
Pattnaik Anandita, Lim Alexandra, Sabeti Sara, Kwon Ashley, Hall Katherine, Lott Ira, Kimonis Virginia
Abstract excerpt
In this report, we describe an unusual case of progressive hemifacial atrophy or Parry-Romberg syndrome in a 10-year-old girl with progressive hemifacial microsomia and limb anomalies who had brain magnetic resonance imaging (MRI) findings of white matter hyper-intensities. Patients typically present with neurological manifestations such as epilepsy, facial pain, and migraines and ophthalmological symptoms in...
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