| PAD | pain and distress; patient surface axis depth; percutaneous abscess drainage; percutaneous automated... |
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| PDQ | Personality Diagnostic Questionnaire; physician's data query; Premenstrual Distress Questionnaire; p... |
| SDCL | symptom distress check list |
| SRD | service-related disability; Society for the Relief of Distress; Society for the Right to Die; sodium... |
| WDHA Syndrome | Watery Diarrhea, Hypokalemia, Achlorhydria Syndrome = Pancreatic Cholera (Syndrome)<... |
| diagnostic techniques, respiratory system | Methods and procedures for the diagnosis of diseases of the respiratory tract or its organs. It includes respiratory function tests. (12 Dec 1998) |
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| external respiratory nerve of Bell | <anatomy, nerve> Arises from the fifth, sixth, and seventh cervical nerves (roots of brachial plexus), descends the neck behind the brachial plexus, and is distributed to the serratus anterior muscle; it is somewhat unusual in that it courses on the superficial aspect of the muscle is supplies; its paralysis results in "winged scapula". Synonym: nervus thoracicus longus, Bell's respiratory nerve, external respiratory nerve of Bell, posterior thoracic nerve. (05 Mar 2000) |
| upper respiratory infection | Any number of viral or bacterial infections that includes infections of the throat, nasopharynx, sinuses, larynx, trachea or bronchi. (27 Sep 1997) |
| upper respiratory tract | The nasopharynx, oral cavity, and throat. (09 Oct 1997) |
| Krause's respiratory bundle | A slender, compact fibre bundle extending longitudinally through the dorsolateral region of the medullary tegmentum, surrounded by the nucleus of the solitary tract, below the obex decussating over the central canal, and descending over some distance into the upper cervical segments of the spinal cord. It is composed of primary sensory fibres that enter with the vagus, glossopharyngeal, and facial nerves, and in part convey information from stretch receptors and chemoreceptors in the walls of the cardiovascular, respiratory, and intestinal tracts; in rostral parts of the tract impulses are generated by the receptor cells of the taste buds in the mucosa of the tongue. Its fibres are distributed to the nucleus of the solitary tract. Synonym: tractus solitarius, fasciculus rotundus, fasciculus solitarius, funiculus solitarius, Gierke's respiratory bundle, Krause's respiratory bundle, round fasciculus, solitary bundle, solitary fasciculus. (05 Mar 2000) |
| lower respiratory tract | <anatomy> The trachea, bronchi, and lungs. (09 Oct 1997) |
| lower respiratory tract smear | A group of cytologic specimens containing material from the lower respiratory tract and consisting mainly of sputum (spontaneous, induced) and material obtained at bronchoscopy (aspirated, lavaged, brushed); used for cytologic study of cancer and other diseases of the lungs. Synonym: bronchoscopic smear, sputum smear. (05 Mar 2000) |
| Aarskog-Scott syndrome | A syndrome of ocular hypertelorism, anteverted nostrils, broad upper lip, saddle-bag scrotum, and laxity of ligaments resulting in genu recurvatum, flat feet, and hyperextensible fingers; X-linked and autosomal dominant forms. Synonym: Aarskog-Scott syndrome. (05 Mar 2000) |
| Aarskog syndrome | <syndrome> Grier et al. (1983) reported father and 2 sons with typical Aarskog syndrome, including short stature, hypertelorism, and shawl scrotum. They tabulated the findings in 82 previous cases. X-linked recessive inheritance has been repeatedly suggested. The family reported by Welch (1974) had affected males in 3 consecutive generations. Thus, there is either genetic heterogeneity or this is an autosomal dominant with strong sex-influence and possibly ascertainment bias resulting from use of the shawl scrotum as a main criterion. Stretchable skin was present in the cases of Grier et al. (1983). Teebi et al. (1993) reported the case of an affected mother and 4 sons (including a pair of monozygotic twins) by 2 different husbands. They suggested that the manifestations were as severe in the mother as in the sons and that this suggested autosomal dominant inheritance. Actually, the mother seemed less severely affected, compatible with X-linked inheritance. Clinical signs: Mild to moderate short stature,normocephaly, Widow's peak hair, maxillary hypoplasia, broad nasal bridge, anteverted nostrils, long philtrum, broad upper lip, curved linear dimple below the lower lip, hypertelorism, ptosis, down-slanted palpebral fissures, ophthalmoplegia, strabismus, hyperopic astigmatism, large cornea, floppy ears, lop-ears,cleft lip/palate, shawl scrotum, saddle-bag scrotum, cryptorchidism, brachydactyly, digital contractures, clinodactyly, mild syndactyly, transverse palmar crease, lymphoedema of the feet, ligamentous laxity, osteochondritis dissecans, proximal finger joint hyperextensibility, flexed distal finger joints, genu recurvatum, flat feet, stretchable skin, cervical spine hypermobility, odontoid anomaly, macrocytic anaemia, hemochromatosis, hepatomegaly, portal cirrhosis, imperforate anus, rectoperineal fistula, interstitial pulmonary disease, sternal deformity. Inheritance: Sex-influenced autosomal dominant form, also X-linked form. (05 Aug 1998) |
| abdominal muscle deficiency syndrome | <syndrome> Congenital absence (partial or complete) of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall; in males, genitourinary anomalies (urinary tract dilation and cryptorchidism) are also found; genetics unclear. (05 Mar 2000) |
| abstinence syndrome | <syndrome> A constellation of physiologic changes undergone by persons or animals who have become physically dependent on a drug or chemical due to prolonged use at elevated doses, but who are abruptly deprived of that substance. The abstinence syndrome varies with the drug to which dependence has developed. Generally the effects observed are in an opposite direction from those produced by the drug; e.g., the withdrawal syndrome from central nervous system depressants such as barbiturates and benzodiazepines consists of insomnia, restlessness, tremulousness, hallucinations, and, in the extreme, tonic-clonic convulsions which may prove fatal. The onset time and severity of the abstinence syndrome depend upon how rapidly the drug disappears from the body. (05 Mar 2000) |
| Achard syndrome | <syndrome> Arachnodactyly with small receding mandible, broad skull, and joint laxity limited to the hands and feet; genetics unclear. (05 Mar 2000) |
| Achard-Thiers syndrome | <syndrome> One form of a virilizing disorder of adrenocortical origin in women, characterised by masculinization and menstrual disorders in association with manifestations of diabetes mellitus, such as glucosuria. (05 Mar 2000) |
| Achenbach syndrome | <syndrome> Haematoma of the finger pad with accompanying oedema; of unknown cause in the absence of disturbances in blood coagulation mechanisms. (05 Mar 2000) |
| achoo syndrome | <syndrome> A disorder characterised by nearly uncontrollable paroxysms of sneezing provoked in a reflex fashion by the sudden exposure of a dark-adapted subject to intensely bright light, usually sunlight. Inheritance: autosomal dominant. (05 Aug 1998) |