hrp0094p2-340 | Multisystem endocrine disorders | ESPE2021
Lassoued Najoua
, Salem Houda Ben
, Ayadi Younes
, Hmida Nada
, Zantour Baha
, Alaya Wafa
, Habib Sfar Mohamed
,
Introduction: Fanconi anemia (FA) is a very rare, complex and chronic genetic disorder. The diagnosis is most often made at pediatric age. Hematopoietic stem cell transplantation (HSCT) is the only curative treatment for bone marrow failure. FA on its own as well as its treatment can affect the endocrine system. We report the case of a child followed for 12 years after HSCT for FA.Observation: A patient has been followed since the age of...