Apert Syndrome: What Is It, Symptoms, Diagnosis & Treatment
Apert syndrome is a rare genetic condition that causes a baby's skull, face, feet and hands to form atypically when the skull joints close too soon.
Apert Syndrome Before & After Pictures in Dallas, TX
Apert syndrome occurs whenever there is a premature fusing of cranial sutures during pregnancy. Resulting in retruded features, Apert syndrome requires surgery to correct deformities and promote normal functioning. The International Craniofacial Institute in …
Apert Syndrome: Symptoms, Causes, Diagnosis ... - WebMD
2022年12月6日 — Babies with Apert syndrome are born with a distorted shape of the head and face. Many children with Apert syndrome also have other birth defects. Apert syndrome has no cure, but surgery can...
Apert Syndrome - Children's Hospital of Philadelphia
Apert syndrome, also called acrocephalosyndactyly, is a genetic syndrome characterized by anomalies of the skull, face and limbs. Gene mutations are responsible for causing the early fusion of the skull, hand and feet bones.
Apert Syndrome - Symptoms, Causes, Treatment | NORD
2019年7月30日 — Apert syndrome is a rare genetic condition that is apparent at birth. People with Apert syndrome can have distinctive malformations of the skull, face, hands, and feet. Apert syndrome is characterized by craniosynostosis, a condition in which the fibrous joints (sutures) between bones of the skull close prematurely.
Apert Syndrome - Boston Children's Hospital
Apert syndrome, also known as acrocephalosyndactyly, is a genetic disorder that causes fusion of the skull, hands, and feet bones. It is characterized by deformities of the skull, face, teeth, and limbs. Apert syndrome occurs in one out of every 65,000 to 88,000 births. Dr. Amir Taghinia, MD: plastic and reconstructive surgeon. Questions?
Apert Syndrome: Causes, Treatments, Symptoms and More
2017年10月18日 — Apert syndrome is a rare, genetic condition in which the joints in a newborn baby’s skull close too early. This is called craniosynostosis. Typically, the fibrous joints in a newborn’s skull...
Apert Syndrome - Seattle Children's
Most often, babies with Apert syndrome have the following characteristics: The upper part of the face is flat. The middle of the face looks sunken in (concave). The eyes look big and may stick out. When the jaws close, the upper jaw is behind the lower jaw (underbite).
Apert Syndrome - Division of Plastic and Reconstructive Surgery
Apert syndrome is a rare genetic condition affecting primarily the skull and facial bones and the limbs. It leads to craniosynostosis, involving the coronal sutures, underdevelopment of the facial bones and a very complex pattern of fusion of the fingers and toes.
Apert Syndrome: Symptoms, Causes, Diagnosis, and Treatment
2023年5月11日 — Apert syndrome is a genetic condition that affects an estimated one in 65,000 to 88,000 newborns each year. Common traits in people with Apert syndrome include prematurely fused bones of the skull, fusion of some fingers and toes, among others.