The Allgrove syndrome or triple A is a rare inherited autosomal recessive syndrome. The presence of the clinical triad type alacrima, achalasia and Addison's disease is sufficient for the diagnosis. We report the case of a family, the sister and the brother, respectively 11 and 19 years old, from a 1st degree consanguineous marriage and who presented the characteristic signs of the Allgrove syndrome with 2 features: a growth hormone deficiency for the sister and congenital bone malformations for the brother. To our knowledge these characteristics have not been described previously.