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  • infantile stiff skin syndromes
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  • chronic syndromes
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  • infantile stiff skin syndromes
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  • paraneoplastic syndromes
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POSSUM Pictures of Standard Syndromes and Undiagnosed Malformations
US screen unsharpness ultrasonic, ultrasound; ultrasonography; unconditioned stimulus; unique sequence;...
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USH Usher syndrome
ACS Acute Coronary Syndromes
CMS Congenital Myasthenic Syndromes
EDS EHLERS-DANLOS SYNDROMES
OFDS Oral-Facial-Digital syndromes
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Senear-Usher disease An eruption involving sun-exposed skin, especially the face; the lesions are scaling erythematous macules and blebs, combining the clinical features of both lupus erythematosus and pemphigus vulgaris; bullae are subcorneal; probably a variant of pemphigus foliaceus.
Synonym: Senear-Usher disease, Senear-Usher syndrome.
(05 Mar 2000)
Senear-Usher syndrome An eruption involving sun-exposed skin, especially the face; the lesions are scaling erythematous macules and blebs, combining the clinical features of both lupus erythematosus and pemphigus vulgaris; bullae are subcorneal; probably a variant of pemphigus foliaceus.
Synonym: Senear-Usher disease, Senear-Usher syndrome.
(05 Mar 2000)
Usher, Barney <person> Canadian dermatologist, *1899.
See: Senear-Usher disease, Senear-Usher syndrome.
(05 Mar 2000)
Usher, Charles Howard <person> English ophthalmologist, 1865-1942.
See: Usher's syndrome.
(05 Mar 2000)
Usher's syndrome <syndrome> Autosomal recessive inheritance; the two forms are distinguishable only by linkage data; causing sensorineural heraring loss and retinitis pigmentosa.
(05 Mar 2000)
androgen resistance syndromes A class of disorders associated with 5a-steroid reductase deficiency, testicular feminization, and related disorders.
Compare: steroid 5a-reductase, Reifenstein's syndrome, infertile male syndrome, testicular feminization syndrome.
(05 Mar 2000)
aortic arch syndromes Any of a group of disorders leading to occlusion of the arteries arising from the aortic arch. Such occlusion may be caused by atherosclerosis, arterial embolism, syphilitic or tuberculous arteritis, etc.
(12 Dec 1998)
malabsorption syndromes General term for syndromes of malnutrition due to failure of normal intestinal absorption of nutrients.
(12 Dec 1998)
paraneoplastic syndromes In patients with neoplastic diseases a wide variety of clinical pictures which are indirect and usually remote effects produced by tumour cell metabolites or other products.
(12 Dec 1998)
pathologic startle syndromes A group of disorders characterised by markedly exaggerated startle reflex and other exaggerated stimulus-induced responses. Includes hyperexplexia and probably latah and the jumping Frenchman of Maine syndrome.
(05 Mar 2000)
chromosomal instability syndromes A group of mendelian conditions associated with chromosomal instability and breakage in vitro, they often manifest an increased tendency to certain types of malignancies.
See: Bloom's syndrome, fragile X syndrome, xeroderma pigmentosum.
(05 Mar 2000)
compartment syndromes Conditions in which increased pressure within a limited space compromises the circulation and function of tissue within that space. Compartmentation involves mainly the leg but also involved are the forearm, arm, thigh, shoulder, and buttock. Some of the causes of increased pressure are trauma, tight dressings, haemorrhage, and exercise. Sequelae include nerve compression, paralysis, and contracture.
(12 Dec 1998)
myelodysplastic syndromes Conditions in which the bone marrow shows qualitative and quantitative changes suggestive of a preleukaemic process, but having a chronic course that does not necessarily terminate as acute leukaemia.
(12 Dec 1998)
myeloproliferative syndromes A group of conditions that result from a disorder in the rate of formation of cells of the bone marrow, including chronic granulocytic leukaemia, erythraemia, myelosclerosis, panmyelosis, and erythraemic myelosis and erythroleukaemia.
(05 Mar 2000)
polyposis syndromes <radiology> Inher. Malig. Type familial polyposis coli dom and adenoma Gardner syndrome dom and Turcot syndrome rec CNS Peutz-Jeghers syndrome dom (+) hamartoma Cowden syndrome dom ? juvenile polyposis coli (?) - juvenile Cronkhite-Canada syndrome
(12 Dec 1998)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Usher Syndromes - »õâ Autosomal recessive hereditary disorders characterized by congenital SENSORINEURAL HEARING LOSS and RETINITIS PIGMENTOSA. Genetically and symptomatically heterogeneous, clinical classes include type I, type II, and type III. Their severity, age of onset of retinitis pigmentosa and the degree of vestibular dysfunction are variable.
    Synonyms : Usher Syndrome, Usher Syndrome, Type I, Usher Syndrome, Type II, Usher Syndrome, Type III, Syndrome, Usher, Syndromes, Usher
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