Hypochondroplasia



hypochondroplasia hy·po·chon·dro·pla·sia (hī’pō-kŏn’drō-plā’zhə, -zhē-ə)
n.
Congenital dwarfism similar to but milder than achondroplasia, not familial and not evident until mid-childhood, in which the skull and facial features remain normal.

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  • Hypochromasia

    hypochromasia hy·po·chro·ma·si·a (hī’pō-krō-mā’zē-ə, -zhə) n. See hypochromia.

  • Hypochromatic

    hypochromatic hy·po·chro·mat·ic (hī’pō-krō-māt’ĭk) adj. Containing a small or abnormally low amount of pigment.



  • Hypochromatism

    hypochromatism hy·po·chro·ma·tism (hī’pō-krō’mə-tĭz’əm) n.

  • Hypochromia

    [hahy-puh-kroh-mee-uh] /ˌhaɪ pəˈkroʊ mi ə/ noun, Pathology. 1. an anemic condition due to a deficiency of hemoglobin in the red blood cells. 2. insufficient color or pigmentation. hypochromia hy·po·chro·mi·a (hī’pō-krō’mē-ə) n. An anemic condition in which the percentage of hemoglobin in red blood cells is abnormally low. Also called hypochromasia, hypochromatism. hy’po·chro’mic adj.



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