| CREST Syndrome | 1. Calcinosis cutis 2. Raynaud's phenomenon 3. Esophageal ... |
|---|---|
| CRST Syndrome | 1. Calcinosis 2. Raynaud's Phenomenon 3. Sclerodactyly ... |
| GAP syndrome | Galactorrhea, Amenorrhea, Prolactinoma Syndrome |
| HHH Syndrome | Hyperamnonemia-Hyperornithinemia-Homocitrullinemia Syndrome |
| LAMB Syndrome | Lentigines, Atrial myxoma, Blue nevi Syndrome |
| cataract-oligophrenia syndrome | <syndrome> A rare neurologic disorder characterised by cerebellolental degeneration with mental retardation; autosomal recessive inheritance. Synonym: cataract-oligophrenia syndrome, Marinesco-Sjogren syndrome, Torsten Sjogren's syndrome. (05 Mar 2000) |
|---|---|
| Parsonage-Turner syndrome | A neurological disorder, of unknown cause, characterised by the sudden onset of severe pain, usually about the shoulder and often beginning at night, soon followed by weakness and wasting of various forequarter muscles, particularly shoulder girdle muscles; both sporadic and familial in occurrence with the former much more common; often preceded by some antecedent event, such as an upper respiratory infection, hospitalization, vaccination, or non-specific trauma; usually attributed to a brachial plexus lesion, because the nerve fibres involed are most often derived from the upper trunk, but actually multiple proximal mononeuropathies. Synonym: acute brachial radiculitis, brachial plexitis, brachial plexus neuropathy, Parsonage-Turner syndrome, shoulder-girdle syndrome. (05 Mar 2000) |
| Refetoff syndrome | <syndrome> A condition characterised by goiter and elevated serum level of thyroid hormones without manifestations of thyrotoxicosis, due to target organ unresponsiveness to thyroid hormones. (05 Mar 2000) |
| vibration syndrome | <syndrome> Tingling, numbness, and blanching of the fingers resulting from use of hand-held vibration tools; may persist without further exposure to vibration. (05 Mar 2000) |
| Mauriac's syndrome | <syndrome> Dwarfism with obesity and hepatosplenomegaly in children with poorly controlled diabetes mellitus. (05 Mar 2000) |
| reflex sympathetic dystrophy syndrome | <syndrome> A condition that features a group of typical symptoms, including pain (often burning type), tenderness, and swelling of an extremity associated with varying degrees of sweating, warmth and/or coolness, flushing, discoloration, and shiny skin. (12 Dec 1998) |
| cat's cry syndrome | <paediatrics, syndrome> A congenital human syndrome caused by the loss of part of the short arm of Chromosome 5. The syndrome gets its name from the peculiar cry of afflicted infants, which sounds like the meowing of a cat. The syndrome causes severe retardation and various congenital malformations. (09 Oct 1997) |
| cat's-eye syndrome | <syndrome> Iris colobomas (resembling the vertical pupils of a cat) and anal atresia, associated with an additional acrocentric chromosome; other malformations and mental retardation may be present. Synonym: Schmid-Fraccaro syndrome. (05 Mar 2000) |
| Refsum's syndrome | A genetic disorder of the fatty acid phytanic acid which accumulates and causes a number of progressive problems including polyneuritis (inflammation of numerous nerves), diminishing vision (due to retinitis pigmentosa), and wobbliness (ataxia) caused by damage to the cerebellar portion of the brain (cerebellar ataxia). (12 Dec 1998) |
| Mayer-Rokitansky-Kuster-Hauser syndrome | <syndrome> Primary amenorrhoea, absence of vagina, or presence of a short vaginal pouch, and absence of the uterus with normal karyotype and ovaries. Synonym: Rokitansky-Kuster-Hauser syndrome. (05 Mar 2000) |
| cauda equina syndrome | <syndrome> A clinical syndrome characterised by dull pain in the lower back and upper buttock region, analgesia in the buttocks, genitalia (or thigh), accompanied by a disturbance of bowel and bladder function. (27 Sep 1997) |
| May-White syndrome | <syndrome> Progressive myoclonus epilepsy with lipomas, deafness, and ataxia; probably a familial form of mitochondrial encephalomyopathy. (05 Mar 2000) |
| McArdle's syndrome | Glycogenosis due to muscle glycogen phosphorylase deficiency, resulting in accumulation of glycogen of normal chemical structure in muscle. Synonym: McArdle's disease, McArdle's syndrome, McArdle-Schmid-Pearson disease, myophosphorylase deficiency glycogenosis. (05 Mar 2000) |
| McCune-Albright syndrome | <syndrome> The abnormal development of multiple bones, hormonal disorder and brownish skin lesions. (27 Sep 1997) |
| cavernous sinus syndrome | <syndrome> This condition is characterised by oedema of the eyelids and conjunctivae and paralysis of the third, fourth and sixth cranial nerves. It is due to a cavernous sinus thrombosis. (27 Sep 1997) |