TYROSINEMIA TYPE 1: A CASE REPORT

被引:0
|
作者
Rashad, Mahmoud [1 ,2 ]
Nasser, Carmen [1 ]
机构
[1] King Fahad Cent Hosp, Al Baha, Saudi Arabia
[2] Al Azher Univ, Cairo, Egypt
关键词
D O I
10.1136/archdischild-2019-epa.770
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
P434
引用
收藏
页码:A326 / A326
页数:1
相关论文
共 50 条
  • [21] HEREDITARY ACUTE TYROSINEMIA - CASE-REPORT
    SANJURJO, P
    RODRIGUEZSORIANO, J
    VALLO, A
    BILBAO, F
    LORIDAN, L
    ANALES ESPANOLES DE PEDIATRIA, 1976, 9 (05): : 547 - 552
  • [22] Tyrosinemia type 1 and ADHD like symptoms similarity or comorbidity about a case
    Belhadga, H.
    Elmaataoui, Z.
    Kisra, H.
    EUROPEAN PSYCHIATRY, 2023, 66 : S509 - S510
  • [23] Tyrosinemia type 1 and ADHD like symptoms similarity or comorbidity about a case
    Belhadga, H.
    Elmaataoui, Z.
    Kisra, H.
    EUROPEAN PSYCHIATRY, 2023, 66 : S509 - S510
  • [24] Tyrosinemia Type I in Japan: A Report of Five Cases
    Nakamura, Kimitoshi
    Ito, Michinori
    Shigematsu, Yosuke
    Endo, Fumio
    HEREDITARY TYROSINEMIA: PATHOGENESIS, SCREENING AND MANAGEMENT, 2017, 959 : 133 - 138
  • [25] A novel mutation causing mild, atypical fumarylacetoacetase deficiency (Tyrosinemia type I): a case report
    David Cassiman
    Renate Zeevaert
    Elisabeth Holme
    Eli-Anne Kvittingen
    Jaak Jaeken
    Orphanet Journal of Rare Diseases, 4
  • [26] A novel mutation causing mild, atypical fumarylacetoacetase deficiency (Tyrosinemia type I): a case report
    Cassiman, David
    Zeevaert, Renate
    Holme, Elisabeth
    Kvittingen, Eli-Anne
    Jaeken, Jaak
    ORPHANET JOURNAL OF RARE DISEASES, 2009, 4
  • [27] Case report: Maternal tyrosinemia type 1a under NTBC treatment with tyrosine- and phenylalanine restricted diet in Chile
    Medina, Maria F.
    Arias, Carolina
    Cabello, Juan F.
    De la Parra, Alicia
    Valiente, Alf
    Castro, Gabriela
    Fuenzalida, Karen
    Cornejo, Veronica
    AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2020, 184 (04) : 1009 - 1013
  • [28] Type 1 tyrosinemia in Finland: a nationwide study
    Aarela, Linnea
    Hiltunen, Pauliina
    Soini, Tea
    Vuorela, Nina
    Huhtala, Heini
    Nevalainen, Pasi I.
    Heikinheimo, Markku
    Kivela, Laura
    Kurppa, Kalle
    ORPHANET JOURNAL OF RARE DISEASES, 2020, 15 (01)
  • [29] ATTENTION DEFICIT IN THE PATIENTS WITH TYROSINEMIA TYPE 1
    Pohorecka, M.
    Jakubowska-Winecka, A.
    Biernacka, M.
    Biernacki, M.
    Kusmierska, K.
    Kowalik, A.
    Wolanczyk, T.
    Sykut-Cegielska, J.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2010, 33 : S24 - S24
  • [30] Lifesaving but Tiresome Treatment for Tyrosinemia Type 1
    Ryu, Moon
    Nguyen, Anthony
    Shekhar, Rahul
    Sheikh, Abu Baker
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2022, 117 (10): : S1979 - S1980