Scientific Programme & Abstracts from the International Meeting in Pediatric Endocrinology (IMPE)

impe0096p31 | Bone, Growth Plate and Mineral Metabolism | IMPE2023

PTH resistance in a patient with 2q37 deletion syndrome and Albright hereditary osteodystrophy phenotype

Aziz Mariana , Lincolns Mendoza Muñoz Ronald , Gazek Natalia , Vaiani Elisa , Ciaccio Marta , Sanchez Eduardo , Huckstadt Victoria , Viterbo Gisela

Background: 2q37 deletion syndrome is a rare chromosomal abnormality (OMIM #600430) also called brachydactyly mental retardation syndrome (BDMR), or Albright Hereditary Osteodystrophy-like syndrome (AHO). It is characterized by a wide spectrum of clinical findings including mild to moderate psychomotor developmental delay/intellectual disability, brachydactyly type E, short stature, obesity, hypotonia, characteristic facial dysmorphism, hypermobility /joint di...