What is another word for Primary Hyperoxaluria?
Pronunciation: [pɹˈa͡ɪməɹi hˌa͡ɪpəɹˌɒksɐlˈʊ͡əɹi͡ə] (IPA) 
Primary Hyperoxaluria (PH) is a rare genetic disorder that affects the body's ability to break down certain amino acids, leading to high levels of oxalate in the urine. This can result in the formation of kidney stones and damage to the kidneys and other organs. Other terms used for PH include oxalosis, oxaluria, and hyperoxaluria type 1. Additionally, there are different types of PH (type 1, 2, and 3), all with varying degrees of severity, but they all share the common characteristic of excess oxalate accumulation. Treatment options for PH may include medication, changes to diet, and in severe cases, liver or kidney transplant.
