منابع مشابه
Sporadic cretinism: a dangerous misnomer.
tently lead to the widely-held, and quite erroneous, opinion that the clinical presentation and neurological damage would be the same and, having the same etiology, could be prevented in the same manner. But this is not so. True cretinism can only be avoided by an adequate iodine intake through gestation. This simply requires substituting all household salt, and that available to domestic anima...
متن کاملClinical Remarks on a Case of Sporadic Cretinism
patient, who was kindly sent to me by Dr David Menzies, is suffering from sporadic cretinism?in other words, from the infantile form of myxcedema. She was admitted to the Edinburgh Eoyal Infirmary on March 30th, 1893. At that time, though she did not look more than 2 or 2| years of age, her actual age was 16 years and 4 months. She measured only 29? inches in length, and weighed only 2 st. 5| l...
متن کاملSporadic Meningioangiomatosis: A Series of Three Pediatric Cases
Meningioangiomatosis (MA) is a rare benign, hamartomatous lesion within the leptomeninges and cerebral cortex. Three percent of intractable epileptic patients with tumor develop MA. It may be accompanied with neurofibromatosis type II, or it may occur sporadically. Three patients, age range of 2-16 years old, presented with episodes of seizure. The patients demonstrated no family history or sti...
متن کاملThree Sporadic Cases of Infection due to Salmonella Type Dublin.
In 1926 Pesch reported a case of meningitis due to a Gaertner-like organism. The culture was examined by Bruce White (1926) and was found by him to be identical with an organism sent to him by Dr. J. W. Bigger. This Dublin strain was isolated from a case of fatal fever supervening after a kidney operation. Bruce White (1929) has exhaustively examined the serology of the Dublin strain. He has sh...
متن کاملThree novel F8 mutations in sporadic haemophilia A cases
Hemophilia A (HA) is an X-linked hereditary disorder characterized by bleeding of variable severity through mild, moderate to severe owing to large range of mutations in the Factor VIII (F8) gene (Bowen 2002). All kind of F8 mutations, except repeats, have been reported for HA, in total up to 2370 (Human Genome Mutation Database 2005). A preliminary study was conducted in our lab for identifica...
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ژورنال
عنوان ژورنال: The Lancet
سال: 1909
ISSN: 0140-6736
DOI: 10.1016/s0140-6736(01)34231-9