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  2. 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.

  3. Kaufman oculocerebrofacial syndrome - Wikipedia

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

    Treatment Thyroid hormone replacement, Speech therapy [ 3 ] 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 ...

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

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

    Upslanting palpebral fissures; Skeletal indicators Tapering fingers; Hypotonia; Genetics. ... There is no curative treatment known at present for his condition ...

  5. 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.

  6. Saethre–Chotzen syndrome - Wikipedia

    en.wikipedia.org/wiki/Saethre–Chotzen_syndrome

    Downward slanting palpebral fissures (separation between upper and lower eyelids) [3] Nearsightedness [4] Epicanthal folds (skin folds of the upper eyelid covering the inner corner of the eye) [6] Blepharophimosis (bilateral ptosis with reduced size of eyelid) [6] Optic atrophy [6] Refractory errors [6]

  7. Sotos syndrome - Wikipedia

    en.wikipedia.org/wiki/Sotos_syndrome

    Affected individuals have dysmorphic features, with macrodolichocephaly, downslanting palpebral fissures and a pointed chin. The facial appearance is most notable in early childhood. Affected infants and children tend to grow quickly; they are significantly taller than their siblings and peers, and have an unusually large skull and large head.

  8. Kohlschütter–Tönz syndrome - Wikipedia

    en.wikipedia.org/wiki/Kohlschütter–Tönz_syndrome

    [5] [6] [10] Other physical symptoms that some cases have presented with include broad thumbs and toes, microcephaly, coarse hair, mildly asymmetric skull, up slanting palpebral fissures which is where the outside corners of the eyes are higher than normal, and smooth philtrum which is where the upper lip does not have a dip in the center.

  9. 2p15-16.1 microdeletion syndrome - Wikipedia

    en.wikipedia.org/wiki/2p15-16.1_microdeletion...

    [1] [2] [3] The shared clinical features include moderate to severe intellectual disability and similar facial features including telecanthus, drooping eyelids, downslanting, short palpebral fissures, a prominent nasal bridge, high palate with long, smooth philtrum and an everted lower lip.

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