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  2. Pfeiffer syndrome - Wikipedia

    en.wikipedia.org/wiki/Pfeiffer_syndrome

    A baby with Pfeiffer syndrome may have a small, beak-shaped nose; crowded, crooked teeth; and sleep apnea, due to nasal blockage. There are three main types of Pfeiffer syndrome: type I is the mildest and most common; type II is the most severe, with neurological problems and a cloverleaf deformity; and type III is similar to type II, but ...

  3. Prince's ex-wife on losing their baby together: 'I don't ...

    www.aol.com/article/entertainment/2017/03/15/...

    Prince's ex-wife Mayte Garcia opened up in a new interview with People to talk about her time with the late singer. Prince's ex-wife on losing their baby together: 'I don't think he ever got over ...

  4. Prince (musician) - Wikipedia

    en.wikipedia.org/wiki/Prince_(musician)

    According to García, she and Prince had a son named Amiir (born October 16, 1996), who died a week after being born due to Pfeiffer syndrome. Attempts by publications to independently verify the child's name, birth, and cause of death proved difficult due to Prince's focus on privacy.

  5. Mayte Garcia - Wikipedia

    en.wikipedia.org/wiki/Mayte_Garcia

    When she was 19, Prince instructed her to get on birth control thus beginning their sexual relationship. After a four-year courtship, they married on February 14, 1996. Their only child, Amiir, was born with Pfeiffer syndrome type 2 on October 16, 1996.

  6. Paternal age effect - Wikipedia

    en.wikipedia.org/wiki/Paternal_age_effect

    These conditions are Apert syndrome, Crouzon syndrome, Pfeiffer syndrome, achondroplasia, thanatophoric dysplasia, multiple endocrine neoplasia type 2, and multiple endocrine neoplasia type 2b. The most significant effect concerns achondroplasia (a form of dwarfism ), which might occur in about 1 in 1,875 children fathered by men over 50 ...

  7. 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

  8. Waardenburg syndrome - Wikipedia

    en.wikipedia.org/wiki/Waardenburg_syndrome

    Medical genetics. Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye ), a white forelock or patches of light skin.

  9. Prince Louis of Wales - Wikipedia

    en.wikipedia.org/wiki/Prince_Louis_of_Wales

    Prince Louis. Prince Louis of Wales ( / ˈluːi / LOO-ee; [1] Louis Arthur Charles; born 23 April 2018) is a member of the British royal family. He is the third and youngest child of William, Prince of Wales, and Catherine, Princess of Wales. A grandson of Charles III, he is fourth in the line of succession to the British throne .

  10. Craniosynostosis - Wikipedia

    en.wikipedia.org/wiki/Craniosynostosis

    Muenke syndrome: coronal craniosynostosis (plagiocephaly and brachycephaly), short feet and palms, hearing impairment, hypertelorism, and proptosis. Pfeiffer syndrome: abnormalities of the skull, hands, and feet; wide-set, bulging eyes, an underdeveloped upper jaw, beaked nose.

  11. Fibroblast growth factor receptor 1 - Wikipedia

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

    Fibroblast growth factor receptor 1 (FGFR1), also known as basic fibroblast growth factor receptor 1, fms-related tyrosine kinase-2 / Pfeiffer syndrome, and CD331, is a receptor tyrosine kinase whose ligands are specific members of the fibroblast growth factor family.