ba0006p107 | (1) | ICCBH2017
Doulgeraki A.
, Costantini A.
, Kampe A.
, Karavitakis E.
, Jantti N.
, Krallis P.
, Athanasopoulou H.
, Xaidara A.
, Makitie O.
Background: Mutations in the PLS3 gene, encoding plastin 3, cause X-linked osteoporosis. Osteoporosis is characterized by low bone mineral density (BMD) and increased susceptibility to fractures. Here we describe a 7-year-old boy with osteoporosis due to a novel PLS3 deletion.Presenting problem: The patient, born to non-consanguineous parents, had a history of one low-energy long-bone fracture, three vertebral fractures (T5, T6 T8) and kyphosis. DXA scan...