Hawkinsinuria With Direct Hyperbilirubinemia in Egyptian-Lebanese Boy

• Váldodahkkit: Hassan El Khatib (Dahkki), Bilal Asaad (Dahkki), Aisha Zaylaa (Dahkki), Farah Awad (Dahkki), Mariam Sbeity (Dahkki), Sirin Mneimneh (Dahkki), Georges Haber (Dahkki), Zeina Naja (Dahkki), Mariam Rajab (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: Frontiers Media S.A., 2019-03-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

Tyrosinemia type III is the rarest type of tyrosinemia, because of a mutation in 4-OH-phenylpyruvate dioxygenase (HPD). This causes two different types of diseases with different modes of inheritance: tyrosinemia type III and hawkinsinuria. Hawkinsinuria is an autosomal dominant disease, which prese...