Familial dysautonomy (Riley-Day syndrome)

Author:

Silva Edward R. Tonholo1,Takahashi Setsuko Ikeda1,Yoshinaga Lucia1

Affiliation:

1. Faculdade de Medicina de Marília

Abstract

Familial dysautonomia, also known as Riley-Day syndrome, is a disorder of autonomic nervous system with an autosomal recessive mode of inheritance. Reduction and/or loss of unmyelinated and small myelinated fibers is found, as reduction of dopamine beta-hydroxylase in blood. The diagnosis is based on clinical features: diminished lacrimation, insensitivity to pain, poor temperature control, abolished deep tendon reflexes, postural hypotension, vomiting attacks, poor motor coordenation, and mental retardation. The treatment is symptomatic and many children die during the first years of life, usually as a result of repeated aspiration pneumonia. We report the case of a 1 year-old child with familial dysautonomia.

Publisher

FapUNIFESP (SciELO)

Subject

Neurology,Clinical Neurology

Reference8 articles.

1. Nerve conduction in familial dysautonomia (Riley-Day syndrome);Brown JC;JAMA,1967

2. Peripheral Neuropathy;Dyck PJ,1984

3. Spinal cord changes in familial dysautonomia;Fogelson MH;Arch Neurol,1967

4. Sensory, motor and autonomic dysfunction: the nervous system in familial dysautonomia;Pearson J;Neurology,1971

5. Central autonomic dysfunction with defective lacrimation: I. Report of five cases;Riley CM;Pediatrics,1949

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1. Riley-Day syndrome;Radiopaedia.org;2020-11-06

2. Neuromuscular Disorders;Self-Assessment Questions for Clinical Molecular Genetics;2019

3. Autonomic Disorders and the Eye;Journal of Neuro-Ophthalmology;2005-03

4. Heat stroke in familial dysautonomia;Pediatric Neurology;2003-08

5. A Review of Self-Injurious Behavior and Pain in Persons with Developmental Disabilities;International Review of Research in Mental Retardation;1997

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