Congenital Porencephaly in a New Born Child
نویسندگان
چکیده
منابع مشابه
Congenital Hydronephrosis in a New-born Infant
The patient, a girl of seventeen years, was admitted to the MIater Infirmnorum Hospital on 3rd November, 1933, as a case of acute appendicitis. She gave a typical history of abdominial pain follovwed by nausea and vomiting, the pain later settling down in the right iliac fossa, where, on admissioni, she was tender and rigid. Immecliate operation was decided onl. At operationi niothing unusual w...
متن کاملSchmallenberg Virus in Calf Born at Term with Porencephaly, Belgium
To the Editor: From the end of August through the end of October 2011, a clinical syndrome involving adult cattle and the fetuses of pregnant cows emerged in the border area between the Netherlands and North Rhine-Westphalia, Germany (1). The syndrome was characterized by nonspecifi c clinical signs (fever, decreased milk production), severe diarrhea, and some abortions. A metagenomic analysis ...
متن کاملCongenital Trypanosomiasis in Child Born in France to African Mother.
References 1. Dick GW, Kitchen SF, Haddow AJ. Zika virus isolations and serological specificity. Trans R Soc Trop Med Hyg. 1952;46: 509–20. http://dx.doi.org/10.1016/0035-9203(52)90042-4 2. Lanciotti RS, Kosoy OL, Laven JJ, Velez JO, Lambert AJ, Johnson AJ, et al. Genetic and serologic properties of Zika virus associated with an epidemic, Yap State, Micronesia, 2007. Emerg Infect Dis. 2008;14:1...
متن کاملA Case of Neurotibromatosis in A 5-Month New Born
SUMMARY Neurofibromatosis, an autosomal dominant disorder is characterized by showan cell tumor affecting any Part of the body containing such cell, giving rise to appropriate fealture according to the organ involved but the most characteristic clinical aspect of the disease is pripheral or cranial nerve tumors usually associated with cafe au lait spots more than 6 in number and larger than 1....
متن کاملCongenital Adrenal Hyperplasia and Schmid Metaphyseal Chondrodysplasia in a Child
Congenital adrenal hyperplasia (CAH) is a group of hereditary diseases, which are autosomal recessive. CAH occurs due to defect in one of the cortisol coding genes and often clinically presents itself with signs of androgen overproduction. In this article, we report a case of CAH and Schmid metaphyseal dysplasia. Our literature review indicated that this report is the first attempt on CYP11B1 a...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
سال: 2014
ISSN: 2249-782X
DOI: 10.7860/jcdr/2014/9981.5140