No abstract available.
Hemangioma* ; Knee*

No abstract available.
Tibia*

No abstract available.

Progressive Muscular Dystrophy is a hereditary disorder characterized by progressive weakness and wasting of muscules. The etiology of muscular dystrophy is unknown, and no from of pharmacological treatment is considered effective. We report 2 cases of progressive muscular dystrophy occuring in a family, which were diagnosed by clinical findings, serum enzyme study and electromyography.
Electromyography ; Humans ; Muscular Dystrophies

No abstract available.
Hydronephrosis* ; Teratoma*

No abstract available.
Chondrogenesis* ; Ear*

We report on a case of right thalamic hemorrhage resulting from low-voltage electrical injury caused by contact between a wet hand and an electronic scale. The patient was treated with clopidogrel for control of a previous cerebral infarction. The patient complained of numbness of the left upper extremity. On neurological examination, decreased motor power of her left side, grade IV, was observed. Findings on computerized tomography of the brain revealed a right thalamic hemorrhage. To the best of our knowledge, cerebral hemorrhage resulting from low-voltage electrical injury has not been previously reported in the literature.
Brain ; Cerebral Hemorrhage ; Cerebral Infarction ; Electric Injuries ; Electronics ; Electrons ; Hand ; Hemorrhage ; Humans ; Hypesthesia ; Neurologic Examination ; Ticlopidine ; Upper Extremity

No abstract available.
Adenomatous Polyposis Coli* ; Colectomy* ; Humans ; Polyps*

Aneurysms arising from the posterior circulation are relatively uncommon and are regarded as the most difficult aneurysms for surgical management because of its confined surgical space and complicated blood vessels around brain stem. Twenty cases of posterior circulation aneurysm were operated between Jan. 1984 and July, 1987. At the same period total surgically treated aneurysms were 181 cases. Among 20 cases, aneurysms at the basilar artery bifurcation were 12 cases, 4 cases at the SCA-basilar artery, 3 cases at the distal PICA and one case was at the PCA(P2-P3). Five patients had multiple aneurysms and one patient had concomitant arteriovenous malformation. For the operative management of these 20 cases, direct neck clipping was done in 16 cases and wrapping was done in 4 cases. Surgical outcome was evaluated: "good" in 10 cases, "fair" in 3 cases, "poor" in 6 cases and one patient expired. Surgical consideration of posterior circulation aneurysms was also disussed on the basis of personal experience.
Aneurysm* ; Arteries ; Arteriovenous Malformations ; Basilar Artery ; Blood Vessels ; Brain Stem ; Humans ; Neck ; Pica

DiGeorge syndrome, a developmental defect of the third and fourth pharyngeal pouches, is characterized by aplasia or hypoplasia of the thymus and parathyroid glands and by conotruncal cardiac malformation. This syndrome is usually associated with deletion of long arm in chromosome 22 (22q11-). We experienced a case of partial DiGeorge syndrome in a 2-month-old male who had hospitalized because of recurrent hypocalcemic tetany and tetralogy of Fallot. Immunologic studies revealed the decreased percentage of T lymphocyte and increased percentage of B lymphocyte. Chromosomal study with high resolution banding, showed 46, XY, 22q13 deletion. We report a case of partial Digeorge syndrome with a brief review of literatures.
Arm ; Chromosomes, Human, Pair 22 ; DiGeorge Syndrome* ; Humans ; Infant ; Lymphocytes ; Male ; Parathyroid Glands ; Tetany ; Tetralogy of Fallot ; Thymus Gland