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Results 1 - 10 of 24 for Synostosis
  1. Spondylocarpotarsal synostosis syndrome 
    Spondylocarpotarsal synostosis syndrome is a disorder that affects the development of bones throughout the body. Newborns with this disorder are of approximately normal ...
    https://medlineplus.gov/.../spondylocarpotarsal-synostosis-syndrome - Genetics
  2. Craniosynostosis 
    ... the baby grows Types of craniosynostosis are: Sagittal synostosis (scaphocephaly) is the most common type. It affects ... more common in girls than in boys. Metopic synostosis is a rare form that affects the suture ...
    https://medlineplus.gov/ency/article/001590.htm - Medical Encyclopedia
  3. TWIST1 gene 
    ... 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome. Eur J Hum Genet. 2006 Jan;14( ...
    https://medlineplus.gov/genetics/gene/twist1 - Genetics
  4. Cytochrome P450 oxidoreductase deficiency 
    ... arachnodactyly); bowing of the thigh bones; and radiohumeral synostosis, which is a bone abnormality that locks the ...
    https://medlineplus.gov/...cytochrome-p450-oxidoreductase-deficiency - Genetics
  5. Liebenberg syndrome 
    ... joint dysplasia Brachydactyly-elbow wrist dysplasia syndrome Carpal synostosis with dysplastic elbow joints and brachydactyly Genetic Testing ...
    https://medlineplus.gov/genetics/condition/liebenberg-syndrome - Genetics
  6. Muenke syndrome 
    ... sufficient to cause the disorder. FGFR3-associated coronal synostosis Muenke nonsyndromic coronal craniosynostosis Genetic Testing Registry: Muenke ...
    https://medlineplus.gov/genetics/condition/muenke-syndrome - Genetics
  7. Tarsal-carpal coalition syndrome 
    Tarsal-carpal coalition syndrome is a rare, inherited bone disorder that affects primarily the hands and feet. Several individual bones make up each wrist (carpal ...
    https://medlineplus.gov/.../tarsal-carpal-coalition-syndrome - Genetics
  8. NOG gene 
    The NOG gene provides instructions for making a protein called noggin. This protein is involved in the development of many body tissues, including nerve ...
    https://medlineplus.gov/genetics/gene/nog - Genetics
  9. Bohring-Opitz syndrome 
    Bohring-Opitz syndrome is a rare condition that affects the development of many parts of the body.Most individuals with Bohring-Opitz syndrome have profound ...
    https://medlineplus.gov/genetics/condition/bohring-opitz-syndrome - Genetics
  10. FLNB gene 
    ... gene mutations have been identified that cause spondylocarpotarsal synostosis syndrome, a disorder that affects the development of ... ankles and other signs and symptoms of spondylocarpotarsal synostosis syndrome. More About This Health Condition Several common ...
    https://medlineplus.gov/genetics/gene/flnb - Genetics
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