Polycystic kidney disease in a patient with achondroplasia: case report. Citation:
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Date
2003Author
McLigeyo SO.
Mirza, NB
Estambale, BB
Wamola, IA
Kariuki, N
Onyono, E
Kabiru, M
Piollet
Type
ArticleLanguage
enMetadata
Show full item recordAbstract
Autosomal dominant polycystic kidney disease is a multisystem disease involving many organs. An association with other diseases such as tuberous sclerosis, von Hippel-Lindau disease and Marfan syndrome have been previously described. We describe a 35 year old female with achondroplasia who developed polycystic kidney disease involving both kidneys and progressing to end-stage renal disease. To the best of our knowledge this is the first such case described in the literature. We also delve, briefly, into the possibility of the genes and chromosomes involved in Marfan syndrome, polycystic kidney disease, tuberous sclerosis and achondroplasia playing a role in the co-occurrence of these entities
URI
http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/46577http://www.ncbi.nlm.nih.gov/pubmed/10065200
Citation
S, MKSOG. 2003. Polycystic kidney disease in a patient with achondroplasia: case report.. East African Medical Journal. 2003; 80(1):56 - 58. : University of Nairobi.Publisher
University of Nairobi
Collections
- Faculty of Health Sciences (FHS) [10377]