AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE WITH CONGENITAL HEPATIC FIBROSIS- A CASE REPORT
Journal Title: Journal of Evolution of Medical and Dental Sciences - Year 2018, Vol 7, Issue 44
Abstract
PRESENTATION OF CASE A 11 years old female child presented with pain abdomen and abdominal distension on and off ever since she was 4 years; not associated with vomiting or altered bowel habits. There was no history of fever, dysuria or increased frequency of micturition. She also had decreased growth rate along with impairment of cognition and memory. The child had a history of one episode of hematemesis when she was 9 months old. There was no history of yellowish discoloration of the skin or urine. She was born spontaneously by vaginal delivery and the neo-natal period was uneventful. There was no medically significant family history of any illness running in her family in the previous two generations.
Authors and Affiliations
Kangkana Mahanta, Pronami Borah, Karabi Bora
Keywords
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- EP ID EP549273
- DOI 10.14260/jemds/2018/1074
- Views 73
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