Aug 13, 2014 · Acrodysostosis is a rare genetic disorder characterized by skeletal malformations, growth delays, short stature, and distinctive facial features caused, in part, by underdeveloped (hypoplastic) of certain facial bones, particularly those in the middle portion of the face.

Acrodysostosis is a rare genetic disease characterized by skeletal malformations, growth delays, short stature and distinctive facial features. A characteristic symptom is unusually small hands and feet with short, stubby fingers and toes.

Acrodysostosis refers to a group of genetic disorders of bone growth. Common signs and symptoms include very short fingers and toes, underdeveloped facial bones, a small nose, and short stature. Many individuals with Acrodysostosis …

Acrodysostosis is a rare congenital malformation syndrome which involves shortening of the interphalangeal joints of the hands and feet, intellectual disability in approximately 90% of affected children, and peculiar facies.

Acrodysostosis (pronounced Acro-dis-o-sto-sis) is a rare genetic disease characterised by skeletal malformations, growth delays, short stature and distinctive facial features. We have a database of over 100 people – mostly children and young people – diagnosed with acrodysostosis worldwide.

Acrodysostosis is an extremely rare disorder that is present at birth (congenital). It leads to problems with the bones of the hands, feet, and nose, and intellectual disability. Most people with acrodysostosis have no family history of the disease. However, sometimes the condition is passed down from parent to child.

肢端发育不全症(acrodysostosis，ACRDYS)由学者Maroteaux和Malamut首次报道，又称"Maroteaux-Malamut综合征" 或"肢端骨发育障碍、鼻骨发育不全和精神发育迟滞综合征" ，表现为短指症、面部骨发育不良、鼻骨发育不全和身材矮小，不同程度智力障碍，伴或不伴多种激素抵抗。

Acrodysostosis is an extremely rare disorder that is present at birth (congenital). It leads to problems with the bones of the hands, feet, and nose, and intellectual disability. The skeleton is made up of 206 bones in the adult and contributes to the form and shape of the body.

Acrodysostosis refers to a group of rare skeletal dysplasias that share in common characteristic clinical and radiological features including brachydactyly, facial dysostosis, and nasal hypoplasia. In the past, the term acrodysostosis has been used to …

Acrodysostosis (ADO) refers to a heterogeneous group of rare skeletal dysplasia that share characteristic features including severe brachydactyly, facial dysostosis and nasal hypoplasia. The literature describing acrodysostosis cases has been ...