Primary Hyperkalemic Periodic Paralysis: A Rare but Serious Condition
Introduction: Primary hyperkalemic periodic paralysis (PHPP, also known as Hyperkalemic Periodic Paralysis, HyperKPP, or, more commonly, channelopathies) is an inherited form of muscle weakness caused by alterations in muscle membrane ion channels, leading to an excessive build-up of the electrolyte potassium (K+) in the muscle cells. The prevalence of Primary hyperkalemic periodic paralysis is estimated […]
by: Alamuddin
Phenylketonuria (PKU): Symptoms, Diagnosis, and Treatment
Introduction: Phenylketonuria (PKU) is a rare genetic disorder that affects how the body processes an amino acid called phenylalanine. PKU is a rare disorder, affecting only about 1 in 10,000 to 15,000 newborns in the United States. However, all newborns must be screened for PKU shortly after birth, as early diagnosis and treatment can prevent […]
by: Alamuddin