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  2. Popliteal pterygium syndrome - Wikipedia

    en.wikipedia.org/wiki/Popliteal_pterygium_syndrome

    Bartsocas-Papas syndrome is a form of popliteal pterygium syndrome and is a very rare disease characterized by congenital craniofacial anomalies, popliteal webbing, and genitourinary and musculoskeletal anomalies. It was first described by Dr. Christos Bartsocas and is more specifically an autosomal recessive popliteal pterygium syndrome. [8]

  3. Angelman syndrome - Wikipedia

    en.wikipedia.org/wiki/Angelman_syndrome

    Angelman syndrome (AS) is a genetic disorder that mainly affects the nervous system. [6] Symptoms include a small head and a specific facial appearance, severe intellectual disability, developmental disability, limited to no functional speech, balance and movement problems, seizures, and sleep problems. [6]

  4. Saethre–Chotzen syndrome - Wikipedia

    en.wikipedia.org/wiki/Saethre–Chotzen_syndrome

    Saethre–Chotzen syndrome (SCS), also known as acrocephalosyndactyly type III, is a rare congenital disorder associated with craniosynostosis (premature closure of one or more of the sutures between the bones of the skull). This affects the shape of the head and face, resulting in a cone-shaped head and an asymmetrical face.

  5. Microdontia - Wikipedia

    en.wikipedia.org/wiki/Microdontia

    Males tend to have larger teeth than females, [1] and tooth size also varies by race. [1] Abnormal tooth size is defined by some as when the dimensions are more than 2 standard deviations from the average. [1] Microdontia is when the teeth are abnormally small, and macrodontia is when the teeth are abnormally large.

  6. Long face syndrome - Wikipedia

    en.wikipedia.org/wiki/Long_face_syndrome

    Long face syndrome, also referred to as skeletal open bite, [1] is a relatively common condition characterised by excessive vertical facial development. [2] Its causes may be either genetic or environmental. Long face syndrome is "a common dentofacial abnormality." [3]: 369 [4] Its diagnosis, symptomology and treatments are complex and ...

  7. Fossil of child with Down syndrome hints at Neanderthal ...

    www.aol.com/news/fossil-child-down-syndrome...

    Living among a small band of Neanderthals in what is now eastern Spain was a child, perhaps 6 years old, with Down syndrome, as shown in a remarkable fossil preserving traits in the inner ear ...

  8. FG syndrome - Wikipedia

    en.wikipedia.org/wiki/FG_syndrome

    FG syndrome's major clinical features include physical disability, usually mild; hyperactive behavior, often with a slow personality; severe constipation, with or without structural anomalies in the anus such as imperforate anus; macrocephaly; severe hypotonia; a characteristic facial appearance due to hypotonia, giving a droopy, "open-mouthed" expression, a thin upper lip, a full or pouting ...

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