Diplegia Facial
Mostrando 1-8 de 8 artigos, teses e dissertações.
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1. Guillain-Barré syndrome associated with SARS-CoV-2 infection: a scoping review
SUMMARY BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections can affect the nervous system, triggering problems such as the Guillain-Barre Syndrome (GBS), an association that can bring complications to the patient. OBJECTIVE: This scoping review aimed to clarify the clinical features and analyze patients with GBS associated w
Rev. Assoc. Med. Bras.. Publicado em: 2021-02
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2. Diplegia facial: etiologia, manifestações clínicas, e avaliação diagnóstica
RESUMO Objetivo Diplegia facial (DF) é uma manifestação neurológica rara proveniente de diferentes causas. Este artigo visa avaliar sistematicamente a etiologia, avaliação diagnóstica e tratamento de DF. Método O estudo foi retrospectivo e incluiu 17 pacientes com diagnóstico de FD. Resultados Os pacientes foram diagnosticados como casos de s�
Arq. Neuro-Psiquiatr.. Publicado em: 2015-12
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3. Congenital facial diplegia.
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4. CONGENITAL FACIAL DIPLEGIA
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5. De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1).
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant condition with variable age of onset and severity. Identification of a de novo DNA fragment by probe p13E-11 (D4F104S1) established the diagnosis of new mutation FSHD in 27 of 31 sporadic cases. The clinical data for these certain new mutation cases were as follows: 13 boys, 14 girls; mea
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6. Poland-Möbius syndrome associated with dextrocardia.
A newborn male with Möbius syndrome, Poland anomaly, and dextrocardia is described. This is the second case reported of Poland-Möbius syndrome associated with dextrocardia. The patient presented with strabismus, facial diplegia, difficulty in swallowing, hypoplasia of the left pectoralis major muscle, partial absence of the upper costal cartilages, absence
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7. Giant axonal neuropathy: normal protein composition of neurofilaments.
A 14-year-old boy had progressive weakness and ataxia since two years of age with tightly curled hair, facial diplegia, distal weakness and hypaesthesia, cerebellar syndrome and normal intelligence. He also had distal renal tubular acidosis manifested by metabolic acidosis. Sural nerve ultrastructure showed numerous giant axons packed with neurofilaments. Th
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8. Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.
In 1972, Fried described a large Scottish family affected by X linked mental retardation (XLMR), hydrocephalus, and mild facial dysmorphism. The phenotype has considerable similarity to the MASA syndrome, which results from mutations of the L1CAM gene in Xq28, and this family has since been assumed to be an example of this condition. We have reinvestigated t