| AMI | Acute Myocardial Infarction - Complications(Cx) 1. Early ... |
|---|---|
| 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 |
| 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) |
| Meadows' syndrome | <syndrome> Cardiomyopathy developing during pregnancy or the puerperium. (05 Mar 2000) |
| Patau's syndrome | <embryology, paediatrics, syndrome> A congenital disorder caused by a person having an extra (three copies of) chromosome 13, this disorder causes severe eye, brain and heart defects and is also characterised by a cleft lip and cleft palate. See: trisomy 13 syndrome (09 Oct 1997) |
| Reifenstein's syndrome | <syndrome> Partial androgen sensitivity; a familial form of male pseudohermaphroditism characterised by varying degrees of ambiguous genitalia or hypospadias, postpubertal development of gynaecomastia, and infertility associated with seminiferous tubular sclerosis; cryptorchidism may be present, and Leydig cell hypofunction may lead to impotence in later years; chromosomal studies are usually normal; X-linked recessive or autosomal dominant male-linked trait. (05 Mar 2000) |
| Paterson-Brown-Kelly syndrome | <syndrome> Limited elevation of the eye in adduction, appearing clinically as a paresis of the inferior oblique muscle, due to fascia contracting the superior oblique muscle on the same side. Synonym: Brown's syndrome, Paterson-Brown-Kelly syndrome. (05 Mar 2000) |
| Paterson-Kelly syndrome | <radiology> Iron-deficiency anaemia, oesophageal webs (symptomatic), glossitis, spoon nails, middle-aged females, increased incidence of oesophageal carcinoma, see also: oesophageal webs and rings aka: Patterson-Kelly syndrome (12 Dec 1998) |
| meckel-gruber syndrome | <radiology> Encephalocele, multiple renal cysts (12 Dec 1998) |
| Reiter's syndrome | <syndrome> The combination of arthritis, conjunctivitis and urethritis (occasionally diarrhoea). Occurs mainly in young men. (27 Sep 1997) |
| reiter syndrome | <radiology> Males, associated with GC ??, polyarthritis, feet (Launois deformity ??), SI joints, knees / ankles (joint effusions), urethritis, uveitis / conjunctivitis (12 Dec 1998) |
| Meckel syndrome | A malformation syndrome, lethal in the perinatal period, and characterised by intrauterine growth retardation, sloping forehead, occipital exencephalocele, ocular anomalies, cleft palate, polydactyly, polycystic kidney, and other malformations; autosomal recessive inheritance. Synonym: Meckel syndrome, Meckel-Gruber syndrome. (05 Mar 2000) |
| virus-associated haemophagocytic syndrome | <syndrome> A syndrome closely resembling malignant histiocytosis but potentially reversible, following a herpes group virus infection such as by the Epstein-Barr virus. (05 Mar 2000) |