| PS | pacemaker syndrome; paired stimulation; paradoxical sleep; paraspinal; parasympathetic; Parkinson sy... |
|---|---|
| SS | disulfide; sacrosciatic; saline soak; saline solution; saliva sample; saliva substitute; Salmonella-... |
| SSS | scalded skin syndrome; secondary Sjogren syndrome; sick sinus syndrome; specific soluble substance; ... |
| TS | Takayasu syndrome; Tay-Sachs; temperature sensitivity; temperature, skin; temporal stem; tensile str... |
| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
chromate
| corpus vertebrae | The main portion of a vertebra anterior to the vertebral canal, as distinct from the arches. Synonym: corpus vertebrae. (05 Mar 2000) |
|---|---|
| corpus vesicae biliaris | The main part of the gallbladder terminating in the rounded fundus below and continuing into the neck of the gallbladder above. Synonym: corpus vesicae biliaris, corpus vesicae felleae. (05 Mar 2000) |
| corpus vesicae felleae | The main part of the gallbladder terminating in the rounded fundus below and continuing into the neck of the gallbladder above. Synonym: corpus vesicae biliaris, corpus vesicae felleae. (05 Mar 2000) |
| corpus vesicae urinariae | The portion of the bladder between the apex and fundus. Synonym: corpus vesicae urinariae. (05 Mar 2000) |
| corpus vitreum | The transparent gel that fills the inner portion of the eyeball between the lens (lens, crystalline) and the retina. (12 Dec 1998) |
| prolapse of the corpus luteum | Ectropion of the corpus luteum, due to eversion of the granulosa membrane through the opening in the ruptured follicle; this occurs normally in certain animals. (05 Mar 2000) |
| trabeculae of corpus spongiosum | The fibrous bands interlacing between the vascular spaces of the corpus spongiosum and glans penis. Synonym: trabeculae corporis spongiosi penis. (05 Mar 2000) |
| tunica albuginea of corpus spongiosum | <anatomy> The thick layer of fibrous tissue surrounding the corpus spongiosum penis. It is thinner than the corresponding layer around each corpus cavernosum. Synonym: tunica albuginea corporis spongiosi, fibrous tunic of corpus spongiosum. (05 Mar 2000) |
| fibrous tunic of corpus spongiosum | <anatomy> The thick layer of fibrous tissue surrounding the corpus spongiosum penis. It is thinner than the corresponding layer around each corpus cavernosum. Synonym: tunica albuginea corporis spongiosi, fibrous tunic of corpus spongiosum. (05 Mar 2000) |
| lateral medullary lamina of corpus striatum | A thin, sharply defined layer of fibres separating the putamen from the globus pallidus. Synonym: lamina medullaris lateralis corporis striati. (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) |