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  2. Pfeiffer syndrome - Wikipedia

    en.wikipedia.org/wiki/Pfeiffer_syndrome

    Pfeiffer syndrome is a rare genetic disorder, characterized by the premature fusion of certain bones of the skull ( craniosynostosis ), which affects the shape of the head and face. The syndrome includes abnormalities of the hands and feet, such as wide and deviated thumbs and big toes. Pfeiffer syndrome is caused by mutations in the fibroblast ...

  3. Carpenter syndrome - Wikipedia

    en.wikipedia.org/wiki/Carpenter_syndrome

    Carpenter syndrome. Carpenter syndrome, also called acrocephalopolysyndactyly type II, [1] is an extremely rare autosomal recessive [2] congenital disorder characterized by craniofacial malformations, obesity, syndactyly, and polydactyly. [2] Acrocephalopolysyndactyly is a variation of acrocephalosyndactyly that presents with polydactyly.

  4. Crouzon syndrome - Wikipedia

    en.wikipedia.org/wiki/Crouzon_syndrome

    Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. Because the branchial arches are important developmental features in a growing embryo, disturbances in their development ...

  5. Apert syndrome - Wikipedia

    en.wikipedia.org/wiki/Apert_syndrome

    Apert syndrome. Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified as a branchial arch syndrome, affecting the first branchial (or pharyngeal) arch, the precursor of the maxilla and mandible. Disturbances in the development of the branchial ...

  6. 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.

  7. Marty Feldman - Wikipedia

    en.wikipedia.org/wiki/Marty_Feldman

    Martin Alan Feldman (8 July 1934 [1] – 2 December 1982) was a British actor, comedian and comedy writer. He was known for his prominent, misaligned eyes. [2] [3] [4] He initially gained prominence as a writer with Barry Took on the ITV sitcom Bootsie and Snudge and the BBC Radio comedy programme Round the Horne.

  8. Pokemon, stuffed animals and skull-expanding surgeries: All ...

    www.aol.com/lifestyle/doctors-expanded-6-old...

    Holden was born with Pfeiffer syndrome, which causes the bones in his skull to fuse prematurely. Six-year-old Holden Smith says he has "a trillion" Pokémon cards, but his favorite one is Koraidon ...

  9. Marfan syndrome - Wikipedia

    en.wikipedia.org/wiki/Marfan_syndrome

    Marfan syndrome ( MFS) is a multi-systemic genetic disorder that affects the connective tissue. [6] [7] [1] Those with the condition tend to be tall and thin, with long arms, legs, fingers, and toes. [1] They also typically have exceptionally flexible joints and abnormally curved spines. [1]