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  2. Kleeblattschaedel - Wikipedia

    en.wikipedia.org/wiki/Kleeblattschaedel

    Kleeblattschaedel. Kleeblattschaedel is a rare malformation of the head where there is a protrusion of the skull and broadening of the face. [2] This condition is a severe type of craniosynostosis. [3] The condition can be both isolated or associated with other craniofacial dysostosises. [4] 85% of children with this condition have other ...

  3. Ashley Peldon - Wikipedia

    en.wikipedia.org/wiki/Ashley_Peldon

    2. Relatives. Courtney Peldon (sister) Website. www .ashleypeldonactress .com. Ashley Peldon (born April 2, 1984) is an American actress, starting as a child actress, transitioning to adult roles, then primarily voice acting after 2008. She has many credits for screams provided for sound effects. [1]

  4. Rudolf Arthur Pfeiffer - Wikipedia

    en.wikipedia.org/wiki/Rudolf_Arthur_Pfeiffer

    Rudolf Arthur Pfeiffer (30 March 1931 – 1 June 2012) was a German geneticist. He discovered Pfeiffer syndrome in 1964. [1] Pfeiffer was born in Saarbrücken, Germany, on 30 March 1931. [1] [2] He studied at the Universities of Vienna, Frankfurt, and Heidelberg. [1]

  5. Beare–Stevenson cutis gyrata syndrome - Wikipedia

    en.wikipedia.org/wiki/Beare–Stevenson_cutis...

    Beare–Stevenson cutis gyrata syndrome is a rare genetic disorder characterized by craniosynostosis (premature fusion of certain bones of the skull, sometimes resulting in a characteristic 'cloverleaf skull'; further growth of the skull is prevented, and therefore the shape of the head and face is abnormal) and a specific skin abnormality, called cutis gyrata, characterized by a furrowed and ...

  6. Hyper-IgM syndrome type 2 - Wikipedia

    en.wikipedia.org/wiki/Hyper-IgM_syndrome_type_2

    Hyper-IgM syndrome type 2. Hyper IgM syndrome type 2 is a rare disease. Unlike other hyper-IgM syndromes, type 2 patients identified thus far did not present with a history of opportunistic infections. One would expect opportunistic infections in any immunodeficiency syndrome. The responsible genetic lesion is in the AICDA gene found at 12p13.

  7. Familial exudative vitreoretinopathy - Wikipedia

    en.wikipedia.org/wiki/Familial_exudative_vitreo...

    Familial exudative vitreoretinopathy (FEVR, pronounced as fever) is a genetic disorder affecting the growth and development of blood vessels in the retina of the eye. This disease can lead to visual impairment and sometimes complete blindness in one or both eyes. FEVR is characterized by incomplete vascularization of the peripheral retina.

  8. Grease 2 (soundtrack) - Wikipedia

    en.wikipedia.org/wiki/Grease_2_(soundtrack)

    link. Grease 2: Original Soundtrack Recording is the original motion picture soundtrack for the 1982 film Grease 2 starring Maxwell Caulfield and Michelle Pfeiffer. It was originally released by RSO Records in 1982, with Polydor Records re-issuing it in 1996. Like the film, the soundtrack failed to match the commercial success of its predecessor.

  9. Cleidocranial dysostosis - Wikipedia

    en.wikipedia.org/wiki/Cleidocranial_dysostosis

    Cleidocranial dysostosis ( CCD ), also called cleidocranial dysplasia, is a birth defect that mostly affects the bones and teeth. [1] The collarbones are typically either poorly developed or absent, which allows the shoulders to be brought close together. [1] The front of the skull often does not close until later, and those affected are often ...