hrp0082p2-d1-293 | Bone | ESPE2014
Djermane Adel
, Ladjouze Asmahane
, Ouarezki Yasmine
, Vuillaumier-Barrot Sandrine
, Khodja Benfetima Ali
, Kedji Leila
, Maoudj Abdeljalil
, Berkouk Karima
, Bensmina Menoubia
, Anane Tahar
, Laraba Abdennour
Background: FanconiĀBickel syndrome (FBS) is a rare glycogen storage disease characterized by hepato-renal glycogen accumulation, severe renal tubular dysfunction and impaired glucose and galactose metabolism. We present the case histories of two sisters who were diagnosed with FBS.Case reports: The proband, Lina, was referred to our clinic for growth retardation and abdominal distention aged 27 months. She is the 4th child of consanguineous parents...