Differential (Click to cross reference) agenesis of corpus callosum anticonvulsants anticonvulsants, teratogenicity of anticonvulsants, untoward effects of areflexia arm weakness brachial neuritis brachial neuritis, acute brachial neuritis, bilateral brachial plexus neuropathy brachial plexus neuropathy, bilateral brachial plexus neuropathy, familial brachial plexus neuropathy, recurrent brain weight cardiomyopathy CAT scan children chromosomal abnormality chromosome 17 cleft lip cleft palate cold temperature congenital birth defects congenital heart disease congenital heart disease, CNS complications with congenital malformation congenital malformation, dilantin therapy causing congenital malformation, non CNS cranial volume Craniosynostosis cryptorchidism developmental abnormality of brain developmental retardation differential diagnosis digits, abnormal dilantin dysmorphic ear, abnormal echocardiogram electromyogram facial anomalies facial appearance, abnormal familial feeding disorder fetal alcohol syndrome gene gene mutation genetic counselling genetic linkage genetic neurologic disorders genetic testing head circumference hearing loss hemorrhagic diathesis hepatosplenomegaly heterotopia high arched palate holoprosencephaly hypertelorism hypertrophic cardiomyopathy hypoplastic left heart syndrome hypotelorism hypotonia hypotonia, infants intellectual deficit interpupillary distance joint hypermobility malformation, CNS, congenital malformation, vascular mental retardation micrencephaly microcephaly micrognathia midline defect in children molecular genetics MRI muscle atrophy, focal neck, webbed neurologic disease, diagnoses of neuropathy, hereditary peripheral Noonan Syndrome nose, abnormal obesity pain pain, severe pectus excavatum polyhydramnios Prader-Labhart-Willi syndrome precipitating factors precocious puberty pregnancy, neurologic complications in proximal muscle atrophy puerperium pulmonary stenosis pyramidal tract dysfunction recurrent review article seizure seizure, children seizure, injury following short neck short stature simian crease skin, lesions in neurologic disorders valvulopathy visual impairment vomiting, recurrent weakness weakness, progressive weakness, proximal

Showing articles 0 to 13 of 13 A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium Neurol 100:631-637, Zeng,T.f.,et al, 2023 Craniofacial and Cutaneous Findings Expand the Phenotype of Hereditary Neuralgic Amyotrophy Neurol 57:1963-1968, Jeannet,P.,et al, 2001 Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Congenital Brain Anomalies Associated with the Hypoplastic Left Heart Syndrome Pediatrics 85:984-990, Glauser,T.A.,et al, 1990 Minor Anomalies in Offspring of Epileptic Mothers J Pediatr 112:521-529, 579-5811988., Gaily,E.,et al, 1988 Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979 Tables of Cranial & Orbital Measurements, Cranial Volume, & Derived Indexes in Males & Females From 7 Days to 20 Years of Age Ann Neurol 2:485, Dekaban,A., 1977 Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence (Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975 Hypertelorism (Greigs Synd) Year Book of Pediatric Opthal p. 181-Circa 1972-3., , 1972 Normal Inner Canthal & Outer Orbital Dimensions J Pediatr 74:465, Laestadius,N.,et al, 1969 Diagnostic Significance of Median Facial Anomalies for Holoprosencephaly Pediatr 256, 1964 Aug., DeMeyer,W.,et al, 1964 Patient Travel Distance to Neurologist Visits Neurol 101:e1807-e1820, Lin,C.C.,et al, 2023 Showing articles 0 to 13 of 13