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syndrome |
syndrome |
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| a group of signs and symptoms that occur together and characterize a disease. |
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disease, Capdepont's; Capdepont syndrome; maladie de (dentinogenesis imperfecta) |
maladie de Capdepont |
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disease, Crouzon's; dysostosis, craniofacial; Crouzon's syndrome |
dysostose crânio-faciale; Crouzon (maladie de) |
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| a condition of unknown etiology that is similar to cleidocranial dysostosis but differs in that the clavicles are not affected. |
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syndrome, Aarskog's |
Aarskog (syndrome de) |
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syndrome, Ackerman's |
Ackerman (syndrome d') |
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syndrome, acquired immunodeficiency; AIDS |
sida |
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| AIDS - the abbreviation for acquired immunodeficiency syndrome. |
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syndrome, acute respiratory distress |
syndrome de détresse respiratoire aiguë |
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| is a diffuse pulmonary parenchymal injury associated with noncardiogenic pulmonary edema and resulting in severe respiratory distress and hypoxemic respiratory failure. The pathologic hallmark is diffuse alveolar damage (DAD) but lung tissue rarely is available for a pathologic diagnosis. Therefore diagnosis is made on clinical grounds, |
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syndrome, adaptation |
syndrome d'adaptation |
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syndrome, Albright's |
Albright (syndrome d') |
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| a polyostotic form of fibrous dysplasia, usually associated with precocious puberty in females, endocrine disturbances influencing growth, and brown pigmentation of the skin. |
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syndrome, Apert's |
Apert (maladie d') |
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| craniostenosis characterized by oxycephaly and syndactyly of the hands and feet. Facial manifestations include exophthalmos, high prominent forehead, small nose, and malformation of the mandible and mouth. Also called acrocephalosyndactyly. |
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syndrome, Ascher's |
Ascher (syndrome d') |
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| syndrome consisting of double lip, a redundance of the skin of the eyelids (blepharochalasis), and nontoxic thyroid enlargement. The sagging eyelids are obvious when the eyes are open; the double lip is seen when the patient smiles. |
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syndrome, Avellis' |
Avellis (syndrome d') |
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syndrome, Baader's dermatostomatitis |
Baader (syndrome de) |
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syndrome, Bechterew-Brissaud |
Bechterew-Brissaud (syndrome de) |
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syndrome, Behçet's aphtae; disease, Behcet's |
Behçet (syndrome ou trisyndrome de) |
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| (Behçet's disease), recurrent iritis and aphthous ulcers of the mouth and genitalia. Other manifestations include arthralgia, hydrarthrosis, swelling of the salivary glands, cutaneous eruptions, and central nervous system disorders. |
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syndrome, Bindei's |
Binder (syndrome de) |
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syndrome, Blanchets |
Blanchet Paul (syndrome de) |
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syndrome, Bloch-Sulzberger |
Bloch-Sulzberger (syndrome de) |
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| (incontinentia pigmenti), syndrome in which pigmented skin lesions, defects of the eyes and central nervous system, skeletal anomalies, and hypoplasia of the teeth occur. |
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syndrome, Bonnet-Dechaume and Blanc |
Bonnet-Dechaume et Blanc (syndrome de) |
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syndrome, Bonnets |
Bonnet (syndrome de) |
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