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  2. Opitz G/BBB syndrome - Wikipedia

    en.wikipedia.org/wiki/Opitz_G/BBB_Syndrome

    In some cases of autosomal dominant Opitz G/BBB syndrome, the disease is caused by a mutation in the SPECC1L gene (near the 22q11.2 gene), which helps make cytospin-A. Cytospin-A is a protein imperative to the formation of facial features and is often considered responsible for the cleft lip or palate that Opitz G/BBB syndrome patients will ...

  3. Vici syndrome - Wikipedia

    en.wikipedia.org/wiki/Vici_syndrome

    Vici syndrome, also called immunodeficiency with cleft lip/palate, cataract, hypopigmentation and absent corpus callosum (or absent corpus callosum cataract immunodeficiency), [1] is a rare autosomal recessive [2] congenital disorder characterized by albinism, agenesis of the corpus callosum, cataracts, cardiomyopathy, severe psychomotor retardation, seizures, immunodeficiency and recurrent ...

  4. Cleft lip and cleft palate - Wikipedia

    en.wikipedia.org/wiki/Cleft_lip_and_cleft_palate

    According to CDC, the prevalence of cleft palate in the United States is 6.35/10000 births and the prevalence of cleft lip with or without cleft palate is 10.63/10000 births. [79] The highest prevalence rates for cleft lip, either with or without cleft palate are reported for Native Americans and Asians .

  5. List of ICD-9 codes 740–759: congenital anomalies - Wikipedia

    en.wikipedia.org/wiki/List_of_ICD-9_codes_740...

    This is a shortened version of the fourteenth chapter of the ICD-9: Congenital Anomalies. It covers ICD codes 740 to 759. The full chapter can be found on pages 417 to 437 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1.

  6. Kallmann syndrome - Wikipedia

    en.wikipedia.org/wiki/Kallmann_syndrome

    Cleft palate, cleft lip or other midline cranio-facial defects. [4] Neural hearing impairment [3] Absence of one of the kidneys (unilateral renal agenesis) [3] Skeletal defects including split hand/foot (ectrodactyly), shortened middle finger (metacarpal) [3] or scoliosis [17] Manual synkinesis (mirror movements of hands) [3] Missing teeth ...

  7. Frontonasal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Frontonasal_dysplasia

    Frontonasal dysplasia (FND) is a congenital malformation of the midface. [1] For the diagnosis of FND, a patient should present at least two of the following characteristics: hypertelorism (an increased distance between the eyes), a wide nasal root, vertical midline cleft of the nose and/or upper lip, cleft of the wings of the nose, malformed nasal tip, encephalocele (an opening of the skull ...

  8. Craniofacial cleft - Wikipedia

    en.wikipedia.org/wiki/Craniofacial_cleft

    [9] [10] Around thirty percent occur with other structural variances, and over 500 syndromes have been identified in which clefting is a principal feature. [9] [10] Clefting can result from teratogens, an agent that disrupts embryo development such as, radiation, maternal infection, chemicals, or drugs.

  9. 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.