Pkan Is De Afkorting Van Pantothenate Kinase Associated Neurodegeneration.


This condition is characterized by progressive difficulty with movement, typically beginning in childhood. Pigmentary retinal degeneration is common. Pkan is een erfelijke aandoening van de hersenen.

The Symptoms Vary From Case To Case And.


Tussen de 35 en 50% van de patiënten met nbia. Pkan is de meest voorkomende vorm van nbia. Bij pkan krijgt iemand steeds meer moeite met bewegen.

Nbia Comprises A Group Of Inherited Neurodegenerative Disorders That Are Characterized.


Pkan is een zeer zeldzame ziekte. Hoe vaak het voorkomt is niet precies bekend. Based on the age of onset and rate of progression, individuals with pkan may be.

Pkan Is A Subtype Of Neurodegeneration With Brain Iron Accumulation (Nbia).


De oorzaak is een foutje in een gen. The condition can also be a result of other illnesses. The illness is usually caused by lymphatic vessels that were misshaped at birth, causing obstruction and subsequent enlargement.

Pkan Is The Most Common Type Of Neurodegeneration With Brain Iron Accumulation (Nbia), A Group Of Clinical Disorders Marked By Progressive Abnormal Involuntary Movements, Alterations.


Pkan is an inherited autosomal recessive disorder. The average age for developing symptoms is 13. Because most of our genes exist in pairs (one coming from the mother and one coming from the father), we normally carry two working.