| mid | middle |
|---|---|
| MIP | macrophage inflammatory protein; major intrinsic protein; maximum inspiratory pressure; maximum inte... |
| ML | Licentiate in Medicine; Licentiate in Midwifery; malignant lymphoma; marked latency; maximum likelih... |
| MLAEP | middle latency auditory evoked potential |
| MLR | mean length response; middle latency response; mixed lymphocyte reaction |
| cortical part of middle cerebral artery | <anatomy, artery> See: middle cerebral artery. Synonym: pars corticalis arteriae cerebralis mediae. (05 Mar 2000) |
|---|---|
| posterior wall of middle ear | It contains the opening into the mastoid antrum. Synonym: paries mastoideus cavi tympani, mastoid wall of middle ear, posterior wall of middle ear. (05 Mar 2000) |
| hypothalamus, middle | That middle portion of the hypothalamus containing the arcuate, dorsomedial, and ventromedial nuclei, and the lateral hypothalamic area. (12 Dec 1998) |
| sphenoidal part of middle cerebral artery | sphenoidal part of middle cerebral artery |
| sulcus for middle temporal artery | <anatomy, artery> A vertical groove located above the external acoustic meatus on the external surface of the squamous part of the temporal bone. Synonym: sulcus arteriae temporalis mediae, sulcus for middle temporal artery. (05 Mar 2000) |
| superficial middle cerebral vein | <anatomy, vein> A large vein passing along the line of the sylvian fissure to join the cavernous sinus; it communicates with the superior sagittal sinus and transverse sinus via the superior and inferior anastomotic veins, respectively. Synonym: vena cerebri media superficialis. (05 Mar 2000) |
| deep middle cerebral vein | <anatomy, vein> The vein that accompanies the middle cerebral artery in the depths of the lateral sulcus and empties into the basal vein of Rosenthal. Synonym: vena cerebri media profunda. (05 Mar 2000) |
| insular part of middle cerebral artery | insular part of middle cerebral artery |
| orbital branch of middle meningeal artery | <anatomy, artery> Branch of middle meningeal artery traversing superior orbital fissure and running toward lacrimal gland. See: anastomotic branch of middle meningeal artery to lacrimal artery. Synonym: ramus orbitalis arteriae meningeae mediae. (05 Mar 2000) |
| tegmental wall of middle ear | The superior wall, or roof, of the tympanic cavity, formed by the tegmen tympani of the temporal bone. Synonym: paries tegmentalis cavi tympani, tegmental wall of middle ear. (05 Mar 2000) |
| jugular wall of middle ear | The floor of the tympanic cavity; a thin plate of bone separating the tympanic cavity from the jugular fossa. Synonym: paries jugularis cavi tympani, fundus tympani, inferior wall of tympanic cavity, jugular wall of middle ear. (05 Mar 2000) |
| labyrinthine wall of middle ear | A bony layer separating the middle from the internal ear or labyrinth; it contains the fenestra vestibuli and the fenestra cochleae. Synonym: paries labyrinthicus cavi tympani, labyrinthine wall of middle ear, medial wall of middle ear. (05 Mar 2000) |
| lateral wall of middle ear | The wall formed mainly by the tympanic membrane. Synonym: paries membranaceus cavi tympani, lateral wall of middle ear, membranous wall of middle ear. (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) |