| Potter, Irving White | <person> U.S. Obstetrician, 1868-1956. See: Potter's version. (05 Mar 2000) |
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| schwann's white substance | <anatomy> The substance of the medullary sheath. Source: Websters Dictionary (01 Mar 1998) |
| sclerosis of white matter | <radiology> Type of dysmyelinating disease, hereditary, peripheral nervous system unaffected in some disorders Specific diseases: adrenoleukodystrophy, metachromatic leukodystrophy, spongy degeneration (Canavan), globoid cell (Krabbe) leukodystrophy, Alexander disease, Pelizaeus-Merzbacher disease, Cockayne syndrome (12 Dec 1998) |
| Hilton's white line | A bluish pink, narrow, wavy zone in the mucosa of the anal canal below the pectinate line at the level of the interval between the subcutaneous part of the external sphincter and the lower border of the internal sphincter, said to be palpable. Synonym: Hilton's white line. (05 Mar 2000) |
| Sergent's white line | A pale streak appearing within 30 to 60 seconds after stroking the skin with a fingernail, and lasting for several minutes; regarded as a sign of diminished arterial tension. Synonym: Sergent's white line. (05 Mar 2000) |
| Nicolle's white mycetoma | Mycetoma caused by a species of Aspergillus, and producing relatively large granules, about the size of a pea; infection occurs from barley grain. (05 Mar 2000) |
| deep white layer of superior colliculus | See: gray layer of superior colliculus. (05 Mar 2000) |
| differential white blood count | An estimate of the percentage of white blood cell types which make up the total white blood cell count. (05 Mar 2000) |
| egg white | The white of an egg, especially a chicken's egg, used in cooking. It contains albumin. (12 Dec 1998) |
| egg-white injury | <syndrome> Dermatitis, loss of hair, and loss of muscle coordination, produced in rats by diets containing large amounts of raw egg white, the avidin of which combines with biotin producing a deficiency of the latter. Synonym: egg-white injury. (05 Mar 2000) |
| familial white folded dysplasia | An autosomal dominant condition of the oral cavity characterised by soft, white or opalescent, thickened and corrugated folds of mucous membrane; other mucosal sites are occasionally involved simultaneously. Synonym: familial white folded dysplasia, oral epithelial nevus. (05 Mar 2000) |
| zinc white | <chemical> A mild astringent and topical protectant with some antiseptic action. It is also used in bandages, pastes, ointments, dental cements, and as a sunblock. Pharmacological action: dermatologic agents, sunscreening agents. Chemical name: Zinc oxide (ZnO) (12 Dec 1998) |
| Lee-White method | A method for determining coagulation time of venous blood in tubes of standard bore at body temperature. (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) |