PT  - JOURNAL ARTICLE
AU  - Al-Sayed, Moeen A.
AU  - Asmari, Ali M.
AU  - Rashed, Mohammed S.
TI  - Goldenhar syndrome and hereditary tyrosinemia type 1
DP  - 2002 Dec 01
TA  - Saudi Medical Journal
PG  - 1527--1531
VI  - 23
IP  - 12
4099  - http://smj.org.sa/content/23/12/1527.short
4100  - http://smj.org.sa/content/23/12/1527.full
SO  - Saudi Med J2002 Dec 01; 23
AB  - We report a case of Goldenhar syndrome and hereditary tyrosinemia type 1 (HTT1), to our knowledge an association not previously described. This case further increases the diversity of observations and clinical descriptions of patients with this complex syndrome. We discuss pathogenetic aspects, and demonstrate further evidence of the effectiveness of 2-(2-nitro-4-trifluoromethyl benzoyl)-1,3-cyclohexanedione in the treatment of HTT1.