منابع مشابه
Familial cerebro-macular degeneration and ataxia.
CASE 1 Colin D. (generation E in Fig. 1), born on 9 September 1958, of non-consanguinous parents, was admitted to the Royal Hospital for Sick Children under the care of Professor R. W. B. Ellis in August 1960 with the complaint that since February of that year he had been increasingly unable to walk. The patient was the result of a full-term spontaneous delivery after an uncomplicated pregnancy...
متن کاملSubacute combined degeneration : report of two cases
Subacute combined degeneration ( SCD) due to vitamin B12 deficiency is common in North of Europe but sometimes it is seen in Iran. It can develop before the symptoms of anemia is obvious, with myelin injury and then axon and even neuron destruction in spinal cord, brain, optic and peripheral nerves. In this study two cases are reported; in the first patient, this disease in manifested by vitami...
متن کاملFamilial cases with age-related macular degeneration.
BACKGROUND The pathogenesis of age-related macular degeneration (AMD) remains unknown. Genetic and environmental factors are thought to be associated with AMD. Although some studies have reported familial cases of AMD in the United States, as far as we know, familial cases of AMD have rarely been reported in Japan. CASES We describe three families with two members of each family affected with...
متن کاملNotes of Two Cases of Cerebro-Spinal Fever, Rungpore Jail
4 P.M.?Temp. 105?, pulse 130, resp. 40, other symptoms same as in the morning. Pulse weaker; resp. jeiky and hurried; pain increased in the head ; first sound of the heart nearly inaudible ; had one feculent bilious stool, no vomiting. Continue medicine every 2 hours, mustard plaster to nape. 1 Gth May 1891, 7 a.m., temp. lOo^0. Very weak and prostrated, pulse very frequent and weak, could not ...
متن کاملCerebro-costo-mandibular syndrome: Report of two cases
Cerebro-costo-mandibular syndrome (CCMS) is a rare syndrome that includes a constellation of mandibular hypoplasia and posterior rib defects as its basic features. Additional features can include hearing loss, tracheal cartilage abnormalities, scoliosis, elbow hypoplasia, and spina bifida. Here we report two cases of CCMS and discuss the reported long-term outcome of the disease.
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1924
ISSN: 0035-9157
DOI: 10.1177/003591572401700931