Lola and Nicole were both born with the rare Autosomal Recessive Polycystic Kidney Disease, which causes cysts to appear in the tubes that produce and transport urine and bile.
What does ARPKD stand for?
ARPKD stands for Autosomal Recessive Polycystic Kidney Disease
This definition appears frequently and is found in the following Acronym Finder categories:
- Science, medicine, engineering, etc.
- Asosiasi Rantai Pendingin Indonesia (Indonesian: Cooling Chain Association of Indonesia)
- Automated Recycling Products Incorporated (Stoughton, WI)
- Award Rates of Pay Index
- Anti-Raider and Pirate Intelligence Agency (gaming Escape Velocity: Nova Plug-In)
- Associazione Ricerca e Prevenzione Inculate Amorose
- Association pour le Régime de Prévoyance de l'Industrie, du Commerce et de l'Artisanat de l'Ardèche
- Arkansas Parent Information Exchange
- Agricultural Research Personnel Information System (Agricultural Research Information System; Indian Council of Agricultural Research; India)
- Australian Racing Pigeon Journal (international magazine)
- Autosomal Recessive Polycystic Kidney Disease
- A Retrieval Process Language
- Achievers' Resources Pvt. Ltd (New Delhi, India)
- Adjust Requested Privilege Level
- Adventure Role Playing League
- Agent Relative Polar Localization (artificial intelligence modelling)
- Angle-Resolved Photo-Luminescence
- Annual Review of Population Law
- Anti-Referral Payments Law
- Army Resource Priorities List
- Army Resourcing Priorities List
Samples in periodicals archive:
Her 10-year-old sister Nicole, also had Autosomal Recessive Polycystic Kidney Disease, but can now eat what she likes after a double organ transplant.
At 28 weeks, scans revealed baby Ellie was suffering from autosomal recessive polycystic kidney disease, a genetic disorder which caused her kidneys to get bigger, put strain on her heart, and stopped her lungs growing properly.
88,89) AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE Autosomal recessive polycystic kidney disease is a cystic variant of PKD emerging from mutations in the PKHD1 gene.
7) In this study we propose a diagnostic classification in 5 categories of the entities presenting with glomerular cysts (Table 1): type I, PKD presenting as a GCK variant of autosomal recessive polycystic kidney disease (ARPKD)/ADPKD (with or without liver disease); type II, hereditary GCK synonymous with GCKD.
This leads to different congenital bile duct disorders, such as Caroli disease and syndrome, autosomal recessive polycystic kidney disease, autosomal dominant polycystic kidney disease, congenital hepatic fibrosis, and bile duct hamartomas (BDHs, also known as von Meyenburg complexes).