Results 1 -
10
of
18
for
Robin sequence
- Pierre Robin sequence is a set of abnormalities affecting the head and face, consisting of a small lower jaw (micrognathia), a tongue that is placed further ...
- Pierre Robin sequence (or syndrome) is a condition in which an infant has a smaller than normal lower jaw, a ... The exact causes of Pierre Robin sequence are unknown. It may be ... The lower jaw develops slowly before birth, but may grow faster ...
- ... SOX9 gene cause some cases of isolated Pierre Robin sequence. Individuals with this condition have a small lower ... mouth (a cleft palate). These cases of Pierre Robin sequence are described as isolated because they occur without ...
- ... cancer and developmental disorders such as isolated Pierre Robin sequence . This condition is caused by changes in regions ... particular genes. The enhancers altered in isolated Pierre-Robin sequence control the activity of the SOX9 gene. In ...
- Pierre Robin Syndrome (Nemours Foundation)Birth Defects/Specifics ... Birth Defects ... Nemours Foundation
- ... A particular group of physical features, called Pierre Robin sequence, is common in people with campomelic dysplasia. Pierre Robin sequence includes an opening in the roof of the ...
- ... A particular group of physical features called Pierre Robin sequence is also common in people with Stickler syndrome. Pierre Robin sequence includes an opening in the roof of the ...
- Craniofacial Abnormalities (National Library of Medicine)Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
- Cleft Lip and Palate Surgery (American Association of Oral and Maxillofacial Surgeons) - PDFCleft Lip and Palate/Treatments and Therapies ... Cleft Lip and Palate ... American Association of Oral and Maxillofacial Surgeons ... PDF
- ... OSMED Heterozygous otospondylomegaepiphyseal dysplasia Otospondylomegaepiphyseal dysplasia, autosomal dominant Pierre Robin syndrome with fetal chondrodysplasia WZS Genetic Testing Registry: Otospondylomegaepiphyseal ...