Hawkinsinuria With Direct Hyperbilirubinemia in Egyptian-Lebanese Boy

• Main Authors: Hassan El Khatib (Author), Bilal Asaad (Author), Aisha Zaylaa (Author), Farah Awad (Author), Mariam Sbeity (Author), Sirin Mneimneh (Author), Georges Haber (Author), Zeina Naja (Author), Mariam Rajab (Author)
• Format: Book
• Published: Frontiers Media S.A., 2019-03-01T00:00:00Z.
• Subjects: article
• Online Access: 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...