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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.

  3. Cardiocranial syndrome, Pfeiffer type - Wikipedia

    en.wikipedia.org/wiki/Cardiocranial_syndrome...

    Cardiocranial syndrome, Pfeiffer type is a rare multiple disorder syndrome characterized by congenital heart defects, sagittal craniosynostosis, and severe developmental delay. The condition has been reported in less than 10 patients worldwide. Signs and symptoms. Features of this condition include: Abnormal heart morphology

  4. Acrocephalosyndactyly - Wikipedia

    en.wikipedia.org/wiki/Acrocephalosyndactyly

    Acrocephalosyndactyly. Acrocephalosyndactyly is a group of congenital conditions characterized by irregular features of the face and skull ( craniosynostosis) and hands and feet ( syndactyly ). [1] Craniosynostosis occurs when the cranial sutures, the fibrous tissue connecting the skull bones, fuse the cranial bones early in development.

  5. Human penis size - Wikipedia

    en.wikipedia.org/wiki/Human_penis_size

    Distribution of penis sizes by circumference. 81% of erect penises (green) are between 10 and 13 cm in circumference. [2] While results vary slightly across reputable studies, the consensus is that the mean human penis, when erect, is in the range 12.9–15 cm (5.1–5.9 in) in length.

  6. Fibroblast growth factor receptor 2 - Wikipedia

    en.wikipedia.org/wiki/Fibroblast_growth_factor...

    View/Edit Mouse. Fibroblast growth factor receptor 2 ( FGFR2) also known as CD332 ( cluster of differentiation 332) is a protein that in humans is encoded by the FGFR2 gene residing on chromosome 10. [5] [6] FGFR2 is a receptor for fibroblast growth factor . The protein encoded by this gene is a member of the fibroblast growth factor receptor ...

  7. 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 ...

  8. Micropenis - Wikipedia

    en.wikipedia.org/wiki/Micropenis

    A micropenis is an unusually small penis. A common criterion is a dorsal (measured on top) penile length of at least 2.5 standard deviations smaller than the mean human penis size. [1] A micropenis is stretched penile length equal to or less than 1.9 cm (0.75 in) in term infants, and 9.3 cm (3.67 in) in adults.

  9. Palpebral fissure - Wikipedia

    en.wikipedia.org/wiki/Palpebral_fissure

    Palpebral fissure. Front of left eye with eyelids separated to show medial canthus. (Palpebral fissure, visible but not labeled, is artificially widened.) The palpebral fissure is the elliptic space between the medial and lateral canthi of the two open eyelids. In simple terms, it is the opening between the eyelids.