| FSHSMA | facioscapulohumeral spinal muscular atrophy |
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| OEIS | omphalocele, exstrophy, imperforate anus, spinal defects [complex] |
| PISCES | percutaneously inserted spinal cord electrical stimulation |
| PSMA | proximal spinal muscular atrophy |
| PSP | pancreatic spasmolytic peptide; paralytic shellfish poisoning; parathyroid secretory protein; period... |
| lateral mammary branches of lateral cutaneous branches of thoracic spinal nerves | Branches arising from the lateral cutaneous branches of the ventral primary rami of spinal nerves (intercostal nerves) T-3 to T-6 which run anteriorly to supply the lateral aspect of the breast. Synonym: rami mammarii laterales rami cutanei lateralis nervorum thoracicorum, rami mammarii laterales rami cutanei lateralis nervorum intercostalium, lateral mammary branches of lateral cutaneous branches of intercostal nerves. (05 Mar 2000) |
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| lateral spinal sclerosis | Considered by many to be a subgroup of motor neuron disease; a slowly progressive degenerative disorder of the motor neurons of the cerebral cortex, resulting in widespread weakness on an upper motor neuron basis; spasticity, hyperreflexia, and Babinski signs are present, but not fasciculation potentials, nor any electrodiagnostic evidence of a lower motor neuron lesion. Synonym: lateral spinal sclerosis. (05 Mar 2000) |
| fractional spinal anaesthesia | Insertion of a catheter into the spinal subarachnoid space and leaving it in situ to permit serial intermittent injection of local anaesthetic solution for prolonged spinal anaesthesia. Synonym: fractional spinal anaesthesia. (05 Mar 2000) |
| loops of spinal nerves | Loops of the spinal nerves, connecting ventral primary rami of the spinal nerves. Synonym: ansae nervorum spinalium. (05 Mar 2000) |
| low spinal anaesthesia | Spinal anaesthesia in which the level of sensory denervation extends to the tenth or eleventh thoracic dermatome. (05 Mar 2000) |
| lumbar enlargement of spinal cord | A spindle-shaped swelling of the spinal cord beginning at the level of the tenth thoracic vertebra and tapering into the medullary cone, with maximum thickness opposite the last thoracic vertebra, consequential to the innervation of the lower limb. Synonym: intumescentia lumbalis, lumbar enlargement of spinal cord. (05 Mar 2000) |
| lumbar part of spinal cord | Portion of spinal cord which consists of the five lumbar segments (L1-L5) and from which five pairs of lumbar spinal nerves originate; in the adult it is located in the T10-L1 portion of the vertebral canal, and is enlarged relative to other parts of the cord due to its involvement in innervation of the lower limb. (05 Mar 2000) |
| lumbar segments of spinal cord | The five lumbar segments of the spinal cord which give rise to the five pairs of lumbar spinal nerves and constitute the lumbar part of the spinal cord. Synonym: segmenta medullae spinalis lumbaria. (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) |
| Achard-Thiers syndrome | <syndrome> One form of a virilizing disorder of adrenocortical origin in women, characterised by masculinization and menstrual disorders in association with manifestations of diabetes mellitus, such as glucosuria. (05 Mar 2000) |
| Achenbach syndrome | <syndrome> Haematoma of the finger pad with accompanying oedema; of unknown cause in the absence of disturbances in blood coagulation mechanisms. (05 Mar 2000) |