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h. zos´ter ophthal´micus herpes zoster involving the ophthalmic division of the trigeminal nerve, characterized by a cutaneous vesicular rash on an erythematous base along the nerve path, preceded by lancinating pain, usually accompanied by conjunctivitis and sometimes by keratitis, scleritis, iridocyclitis, extraocular muscle palsies, ptosis, and mydriasis. Called also gasserian ganglionitis, h. ophthalmicus, and ophthalmic zoster.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
h. cortica´lis defor´mans juveni´lis an autosomal recessive disorder beginning in childhood and marked by multiple fractures and bowing of all extremities, by thickening of the frontal, parietal, and occipital bones, by osteoporosis, and by elevated concentrations of serum alkaline phosphatase and of urinary hydroxyproline. Called also juvenile Paget disease, chronic congenital idiopathic hyperphosphatasemia, and familial osteoectasia.
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h.’s of eyebrow supercilia.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
h. cortica´lis generalisa´ta an autosomal recessive disorder, characterized principally by osteosclerosis of the skull, mandible, clavicles, ribs, and diaphyses of long bones, associated with elevated blood alkaline phosphatase; beginning during puberty, it sometimes leads to optic atrophy and perceptive deafness due to nerve pressure exerted by thickening of the base of the skull. Called also hyperphosphatasemia tarda and van Buchem's syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
h.1 the cellular receptor site for histamine responsible for the dilation of blood vessels and the contraction of smooth muscle; abbreviated H1.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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