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  2. Kaufman oculocerebrofacial syndrome - Wikipedia

    en.wikipedia.org/wiki/Kaufman_oculocerebrofacial...

    Kaufman oculocerebrofacial syndrome, also known as blepharophimosis-ptosis-intellectual disability syndrome, is an extremely rare autosomal recessive congenital disorder characterized by severe mental retardation, brachycephaly, upslanting palpebral fissures, eye abnormalities, and highly arched palate.

  3. Palpebral fissure - Wikipedia

    en.wikipedia.org/wiki/Palpebral_fissure

    The fissure may be increased in vertical height in Graves' disease, which is manifested as Dalrymple's sign. It is seen in disorders such as cri-du-chat syndrome. In animal studies using four times the therapeutic concentration of the ophthalmic solution latanoprost, the size of the palpebral fissure can be increased. The condition is reversible.

  4. MEDNIK syndrome - Wikipedia

    en.wikipedia.org/wiki/MEDNIK_Syndrome

    [2] [3] People with MEDNIK syndrome often have a high forehead, upslanting palpebral fissures, a depressed nasal bridge, low-set ears, growth retardation, and brain atrophy apparent upon imaging. [4] The disorder was discovered by Patrick Cossette and his research team from the Université de Montréal.

  5. Bosch–Boonstra–Schaaf optic atrophy syndrome - Wikipedia

    en.wikipedia.org/wiki/Bosch–Boonstra–Schaaf...

    Upslanting palpebral fissures; Skeletal indicators Tapering fingers; Hypotonia; Genetics. This condition is caused by mutations in the NR2F1 gene.

  6. Smith-Kingsmore syndrome - Wikipedia

    en.wikipedia.org/wiki/Smith-Kingsmore_Syndrome

    Smith-Kingsmore syndrome is a rare genetic disorder that is caused by gain-of-function mutation in a gene MTOR.The facial features of this syndrome are triangular face with a pointed chin, frontal bossing, hypertelorism, eyes with downslanting palpebral fissures, a flat nasal bridge, a long philtrum.

  7. Al-Gazali-Donnai-Mueller syndrome - Wikipedia

    en.wikipedia.org/wiki/Al-Gazali-Donnai-Mueller...

    Al-Gazali-Donnai-Mueller syndrome, also known as Hirschsprung's disease, hypoplastic nails, and minor dysmorphic features syndrome [1] is a rare and deadly genetic disorder which is characterized by Hirschsprung's disease, nail and distal limb hypoplasia, flat facies, upslanting palpebral fissures, narrow philtrum, high palate, micrognathia and low-set ears.

  8. Microcephaly lymphoedema chorioretinal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Microcephaly_lymphoedema_c...

    The distinct facial feature include upslanting palpebral fissures, a broad nose with rounded tip, long philtrum with a thin upper lip, pointed chin and prominent ears (Vasudevan 2005) Genetics [ edit ]

  9. Dalrymple's sign - Wikipedia

    en.wikipedia.org/wiki/Dalrymple's_sign

    Dalrymple's sign is a widened palpebral (eyelid) opening, or eyelid spasm, seen in thyrotoxicosis (as seen in Graves' disease, exophthalmic goitre and other hyperthyroid conditions), causing abnormal wideness of the palpebral fissure.

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