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Adie syndrome, also known as Holmes–Adie syndrome, is a neurological disorder characterized by a tonically dilated pupil that reacts slowly to light but shows a more definite response to accommodation (i.e., light-near dissociation). [1] It is frequently seen in females with absent knee or ankle jerks and impaired sweating.
Adams–Stokes syndrome; Adducted thumb syndrome; Adie syndrome; Adiposogenital dystrophy; Adult-onset immunodeficiency syndrome; Advanced sleep phase disorder; Aerotoxic syndrome; Afferent loop syndrome; Aicardi syndrome; Aicardi–Goutières syndrome; AIDS dysmorphic syndrome; Al-Raqad syndrome; Alagille syndrome; Albinism–deafness syndrome ...
This is a list of major and frequently observed neurological disorders (e.g., Alzheimer's disease), symptoms (e.g., back pain), signs (e.g., aphasia) and syndromes (e.g., Aicardi syndrome). There is disagreement over the definitions and criteria used to delineate various disorders and whether some of these conditions should be classified as ...
Holmes–Adie syndrome: HCP Hereditary coproporphyria: HD Huntington's disease: HDL2 Huntington's disease–like 2: HELLP syndrome: Hemolytic anemia, elevated liver enzymes and low platelet count syndrome HeV Infection Hendra virus infection HF Heart failure: HFA High-functioning autism: HFMD Hand, foot, and mouth disease: HFRS
List of medical symptoms. Medical symptoms refer to the manifestations or indications of a disease or condition, perceived and complained about by the patient. [1] [2] Patients observe these symptoms and seek medical advice from healthcare professionals.
Holmes and Adie shared interests in neurology and neuroanatomy, and in 1941 they published separate papers on the condition. The condition now bears their conjoined eponym, Holmes-Adie syndrome. [12] In the period between the wars, Holmes had concurrent appointments at Queen Square, Moorfields Eye Hospital and the Charing Cross Hospital. He was ...
Ross' syndrome consists of Adie's syndrome (myotonic pupils and absent deep tendon reflexes) plus segmental anhidrosis (typically associated with compensatory hyperhidrosis). [ 1 ] It was characterized in 1958 [ 2 ] [ 3 ] by A.T. Ross. [ 4 ]
Dandy–Walker syndrome recessive form; Dandy–Walker malformation with mental retardation, basal ganglia disease, and seizures; Dandy–Walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy; Dandy–Walker syndrome; Daneman–Davy–Mancer syndrome; Darier's disease; Davenport–Donlan syndrome; DAVID syndrome