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  2. Cleft lip and cleft palate - Wikipedia

    en.wikipedia.org/wiki/Cleft_lip_and_cleft_palate

    [1] [2] Cleft lip and cleft palate can often be diagnosed during pregnancy with an ultrasound exam. [1] A cleft lip or palate can be successfully treated with surgery. [1] This is often done in the first few months of life for cleft lip and before eighteen months for cleft palate. [1] Speech therapy and dental care may also be needed. [1]

  3. Classification of cleft lip and cleft palate - Wikipedia

    en.wikipedia.org/wiki/Classification_of_cleft...

    Cleft lip and clip palate is an "umbrella term" for a heterogeneous collection of orofacial clefts. It includes clefting of the upper lip, the maxillary alveolus (dental arch), and the hard or soft palate, in various combinations. The anatomic combinations include: [1] cleft lip [CL] cleft lip and alveolus [CLA] cleft lip, alveolus, and palate ...

  4. Craniofacial cleft - Wikipedia

    en.wikipedia.org/wiki/Craniofacial_cleft

    Within craniofacial disorders and abnormalities, orofacial clefts, and specifically cleft lip (CL) and cleft palate (CP) are the most common in humans. [9] Occurrences of CL/P are most often (around seventy percent of cases) isolated and nonsyndromic, meaning they are not associated with a syndrome or inherited genetic conditions.

  5. Cleft palate incidence by population - Wikipedia

    en.wikipedia.org/wiki/Cleft_palate_incidence_by...

    Cleft lip and/or palate is a congenital abnormality that is seen frequently around the world. On average, about 1 in every 500-750 live births result in a cleft (Hardin-Jones, Karnell, & Peterson-Falzone, 2001).

  6. Van der Woude syndrome - Wikipedia

    en.wikipedia.org/wiki/Van_der_Woude_Syndrome

    However, when growth of the mandibular process is impeded, a lip pit occurs. Lip pits begin to develop on day 36. Cleft lip begins to develop on day 40, and cleft palate emerges on day 50 of development. [3] There are three types of lip pits, which are classified according to their location: midline upper, comissural, and lower lip.

  7. Holoprosencephaly-ectrodactyly-cleft lip/palate syndrome, also simply known as Hartsfield syndrome, is a rare genetic disorder characterized by the presence of variable holoprosencephaly, ectrodactyly, cleft lip and palate, alongside generalized ectodermal abnormalities.