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19. Polycystic kidney (infantile sponge kidney): Difference between revisions
19. Polycystic kidney (infantile sponge kidney) (view source)
Revision as of 13:45, 7 July 2024
, 7 Julyno edit summary
(Created page with "'''Organ''': Kidneys '''Description''': The kidneys contain many very small cysts, only a few (1-2) mm in diameter. They look like holes left after being stabbed with a small needle. '''Diagnosis''': Autosomal recessive polycystic kidney disease '''Causes''': * Autosomal recessive mutation in PKHD1 gene '''Theory''': Autosomal recessive polycystic kidney disease causes renal failure very soon after birth. Patients with this disease also develop liver failure relat...") |
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'''Organ''': Kidneys | [[File:Polycystic kidney disease (infantile type) prep front.jpg|thumb|Polycystic kidney disease (infantile type) prep front]]'''Organ''': Kidneys | ||
'''Description''': | '''Description''': | ||
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Autosomal recessive polycystic kidney disease causes renal failure very soon after birth. Patients with this disease also develop liver failure relatively soon due to the presence of many cysts in the liver too. | Autosomal recessive polycystic kidney disease causes renal failure very soon after birth. Patients with this disease also develop liver failure relatively soon due to the presence of many cysts in the liver too. | ||
[[File:Polycystic kidney disease (infantile type) prep back.jpg|center|thumb|Polycystic kidney disease (infantile type) prep back]] | [[File:Polycystic kidney disease (infantile type) prep back.jpg|center|thumb|Polycystic kidney disease (infantile type) prep back]] | ||
[[Category:Pathology 2 - Macropreparations]] | [[Category:Pathology 2 - Macropreparations]] | ||