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  2. Chin - Wikipedia

    en.wikipedia.org/wiki/Chin

    Cleft chins are common among people originating from Europe, the Middle East and South Asia. [21] There is a possible genetic cause for cleft chins, a genetic marker called rs11684042, which is located in chromosome 2. [22] In Persian literature, the chin dimple is considered a factor of beauty and is metaphorically referred to as "the chin pit ...

  3. Treacher Collins syndrome - Wikipedia

    en.wikipedia.org/wiki/Treacher_Collins_syndrome

    Treacher Collins syndrome (TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. [5] The degree to which a person is affected, however, may vary from mild to severe. [5] Complications may include breathing problems, problems seeing, cleft palate, and hearing loss. [5]

  4. Simple Mendelian genetics in humans - Wikipedia

    en.wikipedia.org/wiki/Simple_Mendelian_genetics...

    Mendelian traits behave according to the model of monogenic or simple gene inheritance in which one gene corresponds to one trait. Discrete traits (as opposed to continuously varying traits such as height) with simple Mendelian inheritance patterns are relatively rare in nature, and many of the clearest examples in humans cause disorders.

  5. Human genetics - Wikipedia

    en.wikipedia.org/wiki/Human_genetics

    Download as PDF; Printable version; ... Human genetics is the study of inheritance as it occurs in human beings. ... Cleft chin: smooth chin [14]

  6. Chromosome 2 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_2

    Download as PDF; Printable version; ... Cleft chin [22] ... Genetics Home Reference. Archived from the original on 9 March 2016

  7. Craniofacial cleft - Wikipedia

    en.wikipedia.org/wiki/Craniofacial_cleft

    [9] [10] Genetic causes are linked with most craniofacial syndromes, and CL/P and other orofacial clefts are recognized as heterogeneous disorders, meaning there are multiple recognized causes. [9] [11] Orofacial clefts have great phenotypic diversity, and their associated genetic environments have called for vast research and investigation.

  8. Hypochondrogenesis - Wikipedia

    en.wikipedia.org/wiki/Hypochondrogenesis

    The face appears flat and oval-shaped, with widely spaced eyes, a small chin, and, in some cases, an opening in the roof of the mouth called a cleft palate. The abdomen is enlarged, and excess fluid may build up in the body before birth (a condition called hydrops fetalis ).

  9. Cerebro-costo-mandibular syndrome - Wikipedia

    en.wikipedia.org/wiki/Cerebro-costo-mandibular...

    Medical genetics: Symptoms: Jaw, rib, and palate anomalies ... Cerebro-costo-mandibular syndrome is a very rare genetic disorder which is characterized by jaw/chin ...