[Tyrosinemia type II. Case report]. / La tyrosinemie type II. A propos d'un cas.

Tyrosinemia type II or Richner-Hanhart syndrome is a rare hereditary disease characterized by the association of pseudoherpetiform corneal ulcerations and palmoplantar hyperkeratosis. We report the case of a 12 year-old young man presenting a superficial punctate keratitis and a corneal dystrophy in both eyes, associated with a palmoplantar hyperkeratosis. The dosage of the serum level of tyrosine is meaningfully raised to 1236 micromol/l. A dietary treatment restraining tyrosine and phenylalanine is started with favorable results after an evolution of 6 months. Tyrosinemia type II is an autosomal recessive disease, due to an enzymatic deficit in tyrosine aminotransferase. The diagnosis is based on the clinic and high level of serum and urinary tyrosine as well as of its urinary metabolites. This disease must be suspected in all cases of dentritic keratitis not reacting on the antiviral treatment, and more especially if it is associated with cutaneous lesions such as palmo-plantar keratosis.

[Marcus-Gunn Syndrome. Based on a case report]. / Syndrome de Marcus-Gunn. A propos d'un cas.

The Marcus-Gunn syndrome associates an unilateral congenital blepharoptosis and "jaw-winking" synkinesia. We report a 12-year-old girl presenting an unilateral Marcus-Gunn syndrome and discuss the clinic, pathogenesis and treatment of this syndrome.