Differential (Click to cross reference) alopecia anticonvulsants ataxia basal ganglia basal ganglia, calcification of basal ganglia, degeneration basal ganglia, lesion of basal ganglia, lesion, bilateral biotin biotin deficiency biotin deficiency, acquired biotin deficiency, juvenile form biotinidase deficiency biotin-responsive basal ganglia disease calcification, intracranial CAT scan CAT scan, abnormal cerebral cortex children choreoathetosis Clinical Pathologic Conference(C.P.C.) coma conjunctivitis deep gray nuclei dermatitis developmental retardation dialysis dementia dysarthria dystonia dystonia, painful encephalopathy enzyme, defect falling familial fever fluctuate gene gene mutation genetic neurologic disorders gyrus, abnormal hearing loss hypotonia infantile bilateral striatal necrosis infantile spasm keratoconjunctivitis lenticular nucleus, lesion of, bilateral lethargy metabolic acidosis metabolic disorder, primary metabolic disorder, primary-screening tests movement disorder movement disorder, extrapyramidal MRI, abnormal MRI, diffusion weighted MRI, disappearing lesion on MRS neuropathology optic atrophy pallor parenteral alimentation polyneuropathy, uremic progressive neurologic disorder rash Saudi Arabia seborrheic dermatitis seizure seizure, children seizure, neonatal skin, lesions in neurologic disorders spasticity striatum, lesion of striatum, lesion of, bilateral symmetric brain lesions tonic foot response treatment of neurologic disorder vitamin deficiency walking, difficulty with wheelchair

Showing articles 0 to 11 of 11 Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3 NEJM 377:2376-2385, Case 38-2017, 2017 MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment Neurol 86:e71-e72, Saeedan, M.B. & Dogar, M.A., 2016 Familial Infantile Bilateral Striatal Necrosis Neurol 59:983-989, Straussberg,R.,et al, 2002 Infantile Spasms as the Initial Symptom of Biotinidase Deficiency J Pediatr 124:103-104, Kalayci,O.,et al, 1994 Basal Ganglia Calcifications in a Case of Biotinidase Deficiency Neurol 38:1326-1328, Schulz,P.E.,et al, 1988 Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program NEJM 313:16-19, 43-441985., Wolf,B.,et al, 1985 Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis Ann Neurol 18:614-617, Wolf,B.,et al, 1985 Impaired Biotin Status in Anticonvulsant Therapy Ann Neurol 12:485-486, Krause,K-H.,et al, 1982 Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin NEJM 304:817-820, Thoene,J.,et al, 1981 Biotin Deficiency:An Unusual Complication Of Parenteral Alimentation NEJM 304:820-823, Mock,D.M.,et al, 1981 Biotin For Neurologic Disorders of Uremia NEJM 304:764, Yatzidis,H.,et al, 1981 Showing articles 0 to 11 of 11