| PMS | patient management system; perimenstrual syndrome; periodic movements during sleep; phenazine methos... |
|---|---|
| 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... |
chromate
| 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) |
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| 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) |
| splenium of corpus callosum | The thickened posterior extremity of the corpus callosum. Synonym: splenium corporis callosi. (05 Mar 2000) |
| sulcus of corpus callosum | The fissure between the corpus callosum and the cingulate gyrus. Synonym: sulcus corporis callosi, callosal sulcus. (05 Mar 2000) |
| dorsal vein of corpus callosum | It originates on the superior surface of the corpus callosum and runs posteriorly to terminate in the great cerebral vein. Synonym: dorsal callosal vein, dorsal vein of corpus callosum, posterior marginal vein, posterior pericallosal vein. (05 Mar 2000) |
| occipital part of corpus callosum | Occipital radiation of the corpus callosum; that part of the fibre radiation of the corpus callosum which bends sharply backward into the occipital lobe of the cerebrum. Synonym: forceps major, forceps posterior, occipital part of corpus callosum, pars occipitalis corporis callosi. (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) |
| trunk of corpus callosum | The main arched portion of the corpus callosum. Synonym: truncus corporis callosi. (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) |
| frontal part of corpus callosum | Frontal radiation of the corpus callosum; that part of the fibre radiation of the corpus callosum which bends forward toward the frontal pole of the cerebrum. Synonym: forceps minor, forceps anterior, frontal part of corpus callosum, pars frontalis corporis callosi. (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) |