1 Table of Contents: “... -- Survival of a Male Infant with a Familial Xp11.4 Deletion Causing Ornithine Transcarbamylase Deficiency...”

2 Table of Contents: “... Spasms in a Male Patient Due to a De Novo ALG13 Gene Mutation -- Liver Failure as the Presentation...”

3 Table of Contents: “... of Phenylalanine and Tyrosine in Phenylketonuria -- Japanese Male Siblings with 2-Methyl-3-Hydroxybutyryl-CoA...”

4 Table of Contents: “...First Successful Conception Induced by a Male Cystinosis Patient -- Glutaric Acidemia Type 1: A...”

5 Table of Contents: “... in Patients with Phenylalanine Hydroxylase Deficiency -- Hypogonadotropic Hypogonadism in Males with Glycogen...”