| FMEN | familial multiple endocrine neoplasia |
|---|---|
| FMFD | V familial multiple coagulation factor deficiency V |
| GPMAL | gravida, para, multiple births, abortions, and live births |
| HMQC | heteronuclear multiple-quantum correlation |
| IFMSS | International Federation of Multiple Sclerosis Societies |
| vater syndrome | <radiology> V vertebral anomalies vascular anomalies, A anal atresia, T tracheo-oesophageal fistula, E oesophageal atresia, R renal anomalies radial dysplasia (12 Dec 1998) |
|---|---|
| Ramsay Hunt's syndrome | <syndrome> An intention tremor beginning in one extremity, gradually increasing in intensity, and subsequently involving other parts of the body. Synonym: progressive cerebellar tremor. Facial paralysis, otalgia, and herpes zoster resulting from viral infection of the seventh cranial nerve and geniculate ganglion, a form of juvenile paralysis agitans associated with primary atrophy of the pallidal system. Synonym: paleostriatal syndrome, pallidal syndrome. Synonym: Ramsay Hunt's syndrome. (05 Mar 2000) |
| gastrocardiac syndrome | <syndrome> Disturbances of the heart's action due to faulty action of the digestive system, especially of the stomach. (05 Mar 2000) |
| malignant carcinoid syndrome | <syndrome> A symptom complex associated with carcinoid tumour and characterised by attacks of severe flushing of the skin, diarrhoeal watery stools, bronchoconstriction, sudden drops in blood pressure, oedema, and ascites. The carcinoid tumours are usually located in the gastrointestinal tract and metastasize to the liver. Symptoms are caused by tumour secretion of serotonin, prostaglandins, and other biologically active substances. Cardiac manifestations constitute carcinoid heart disease. (12 Dec 1998) |
| malignant mole syndrome | <syndrome> Irregularly shaped, variously coloured, distinctively melanocytic, 5 to 10 mm nevi occurring in large numbers (to over 100) primarily on the trunk and extremities, with a high risk of malignancy reported in several members and three generations of a family. (05 Mar 2000) |
| gastrojejunal loop obstruction syndrome | <syndrome> A complication of gastrojejunostomy, caused by acute or chronic obstruction of the afferent loop due to hernia, intussusception, kinking, volvulus, etc. It is characterised by pain and vomiting of bile-stained fluid and includes acute afferent loop obstruction and bilious vomiting. (12 Dec 1998) |
| mallory-weiss syndrome | <syndrome> Mucosal gastric tear, only 10% are purely oesophageal: most are at GE junction or proximal stomach, M greater than F, associated with retching, EtOH, massive haematemesis, abdominal pain, Diagnosis: endoscopy, Treatment: IA vasopressin see: oesophageal trauma (12 Dec 1998) |
| velo-cardio-facial syndrome | <syndrome> Also known as shprintzen syndrome, this more than is a congenital malformation (birth defect) syndrome with cleft palate, heart defect, abnormal face, and learning problems. The condition is therefore called the velo-cardio-facial (vcf) syndrome. (the velum is the soft palate). Other less frequent features include short stature, small-than-normal head (microcephaly), mental retardation, minor ear anomalies, slender hands and digits, and inguinal hernia. The cause is usually a microdeletion in chromosome band 22q11.2, just as in digeorge syndrome. Vcf and digeorge syndromes are different clinical expressions of essentially the same chromosome defect. Of essentially the same chromosome defect. (12 Dec 1998) |
| papillary muscle syndrome | Impaired function of a papillary muscle, usually due to ischemia or infarction, with resulting incompetence of the mitral valve. Synonym: papillary muscle syndrome. (05 Mar 2000) |
| gay bowel syndrome | <syndrome> Gastrointestinal discomfort experienced by homosexual males; includes abdominal pain, cramps, bloating, flatulence, nausea, vomiting, or diarrhoea caused by enteric bacteria, viruses, fungi, zooparasites, or trauma. (05 Mar 2000) |
| Papillon-Leage and Psaume syndrome | <syndrome> An inherited syndrome, lethal in males, with varying combinations of defects of the oral cavity, face, and hands, including lobulated or bifid tongue, cleft or pseudocleft palate, tongue tumours, missing or malpositioned teeth, hypoplastic nasal alar cartilage, depressed nasal bridge, brachydactyly, clinodactyly, incomplete syndactyly, and, frequently, mental retardation. There are two subtypes recognised. Type I (papillon-leage and psaume syndrome, gorlin-psaume syndrome) is inherited as an x-linked dominant trait and is found only in females and XXY males. Type II (mohr syndrome) is inherited as an autosomal recessive trait. Inheritance: autosomal recessive and X-linked. Synonym: OFD syndrome, orofaciodigital syndrome, Papillon-Leage and Psaume syndrome. (05 Mar 2000) |
| Papillon-Lefevre syndrome | <syndrome> A rare congenital hyperkeratosis of the palms and soles (palmoplantar keratoderma), with progessive destruction of the alveolar bone of both the deciduous and permanent teeth. It occurs between the first and fifth years of life and has autosomal recessive inheritance. Inheritance: autosomal recessive. (05 Mar 2000) |
| Gelineau's syndrome | <neurology> A disorder of sleep associated with excessive daytime sleepiness, involuntary daytime sleep episodes, disturbed nocturnal sleep and cataplexy. Narcolepsy affects over 100,000 people in the United States and appears to have a genetic basis. Symptoms usually begin in the patients twenties. Treatment often includes the use of amphetamines and-or tricyclic antidepressants. (27 Sep 1997) |
| mandibulofacial dysotosis syndrome | A hereditary disorder occurring in two forms: the complete form (franceschetti's syndrome) is characterised by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (treacher collins syndrome) is characterised by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (12 Dec 1998) |
| mandibulo-oculofacial syndrome | A syndrome of bony anomalies of the calvaria, face, and jaw, with brachygnathia, narrow curved nose, and multiple ocular defects including microphthalmia, microcornea, and cataract, often with alopecia overlying skull sutures, or alopecia areata and hypoplasia, or absence of eyebrows. The pattern of inheritance is undecided. Synonym: congenital sutural alopecia, Hallermann-Streiff syndrome, Hallermann-Streiff-Francois syndrome, mandibulo-oculofacial syndrome, oculomandibulodyscephaly, oculomandibulofacial syndrome, progeria with cataract, progeria with microphthalmia. (05 Mar 2000) |