| cauda equina syndrome | <syndrome> A clinical syndrome characterised by dull pain in the lower back and upper buttock region, analgesia in the buttocks, genitalia (or thigh), accompanied by a disturbance of bowel and bladder function. (27 Sep 1997) |
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| cauda equina | <anatomy> A bundle of spinal nerve roots which arise from the termination of the spinal cord proper, it comprises the roots of all the spinal nerves below the first lumbar (L1). (16 Mar 1998) |
| Setaria equina | A species that is a common parasite of horses and other equids in all parts of the world; they are slender whitish filaments, several inches in length, usually found free in the peritoneal cavity, but occasionally reported in the pleural cavity, lungs, scrotum, eye, and intestine. (05 Mar 2000) |
| Taenia equina | A cosmopolitan species of the horse, donkey, mule, and zebra; cysticercoid larvae are found in arthropods. Synonym: Taenia equina, Taenia quadrilobata. (05 Mar 2000) |
| cauda | Synonym: tail. Origin: L. A tail (05 Mar 2000) |
| cauda epididymidis | The inferior part of the epididymis that leads into the ductus deferens; part of the reservoir of spermatozoa. Synonym: cauda epididymidis, cauda epididymis, globus minor. (05 Mar 2000) |
| cauda epididymis | The inferior part of the epididymis that leads into the ductus deferens; part of the reservoir of spermatozoa. Synonym: cauda epididymidis, cauda epididymis, globus minor. (05 Mar 2000) |
| cauda fasciae dentatae | A slender whitish band, the attenuated anterior continuation of the dentate gyrus (fascia dentata), crossing transversally the surface of the recurved part of the uncus gyri parahippocampalis. Synonym: band of Giacomini, cauda fasciae dentatae, frenulum of Giacomini, tail of dentate gyrus. (05 Mar 2000) |
| cauda helicis | A flattened process terminating the cartilage of the helix of the ear, posteriorly and inferiorly. Synonym: cauda helicis. (05 Mar 2000) |
| cauda nuclei caudati | The elongated posterior extension of the caudate nucleus that parallels the body and inferior horn of the lateral ventricle. Synonym: cauda nuclei caudati, cauda striati. (05 Mar 2000) |
| cauda pancreatis | The left extremity of the pancreas within the lienorenal ligament. Synonym: cauda pancreatis. (05 Mar 2000) |
| cauda striati | The elongated posterior extension of the caudate nucleus that parallels the body and inferior horn of the lateral ventricle. Synonym: cauda nuclei caudati, cauda 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) |