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Computed tomography shows a small hematoma in the right cerebellum. (Contributed by Dr. Ravindra Kumar Garg.)
May. 16, 2020
Childhood Degenerative & Metabolic Disorders
Feb. 06, 2020
Headache & Pain
Hemicrania continua is characterized by unilateral, continuous headache with ipsilateral ptosis, miosis, tearing, nasal congestion, and facial sweating. It is an indomethacin-responsive trigeminal autonomic cephalgia often clustering in a seasonal pattern and accompanied by continuous background pain between flare-ups.
Feb. 18, 2021
General Child Neurology
Apr. 20, 2020
Charcot-Marie-Tooth disease type 1B is characterized by slowly progressive peripheral nerve manifestations with distal dominant weakness, sensory loss, and limb deformities. It has an autosomal dominant inheritance pattern and is caused by mutations in the myelin protein zero gene.
Aug. 20, 2019
Tyrosine hydroxylase deficiency is an autosomal recessively inherited inborn error of metabolism that involves the biosynthesis of catecholamines (dopamine,
Jul. 08, 2015
Behavioral & Cognitive Disorders
PANDAS is characterized by acute onset of obsessive-compulsive symptoms, tics, behavioral and motor regression, following streptococcal infection. Immune-mediated autoaggressive attack on basal ganglia antigens is believed to be involved.
Dec. 01, 2020
Aug. 14, 2021