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  2. Blepharophimosis, ptosis, epicanthus inversus syndrome

    en.wikipedia.org/wiki/Blepharophimosis,_ptosis...

    Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) is a rare medical anomaly characterized by the conditions it is named after: blepharophimosis, ptosis and epicanthus inversus. There are two types; type 1 is distinguished from type 2 by including the symptom of premature ovarian insufficiency (POI) in females, which causes ...

  3. Blepharophimosis intellectual disability syndromes - Wikipedia

    en.wikipedia.org/wiki/Blepharophimosis...

    Also known Blepharophimosis-intellectual disability syndrome, Ohdo type, it is a very rare type of BIDS that is characterized by blepharophimosis, ptosis, intellectual disabilities, hearing loss, and underdevelopment of teeth. Autosomal recessive, dominant, X-linked recessive, and mitochondrial inheritance patterns have been suggested.

  4. Blepharophimosis - Wikipedia

    en.wikipedia.org/wiki/Blepharophimosis

    Blepharophimosis forms a part of blepharophimosis, ptosis, epicanthus inversus syndrome (BPES), also called blepharophimosis syndrome, which is an autosomal dominant condition characterised by blepharophimosis, ptosis (upper eyelid drooping), epicanthus inversus (skin folds by the nasal bridge, more prominent lower than upper lid) and telecanthus (widening of the distance between the inner ...

  5. 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 ...

  6. Blepharophimosis-ptosis-esotropia-syndactyly-short stature ...

    en.wikipedia.org/wiki/Blepharophimosis-ptosis...

    Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome is a very rare genetic and congenital disorder which is characterized by blepharophimosis, ptosis, V-esotropia, foot syndactyly, extra-ocular and frontal muscles weakness, low height/short stature, prognathism, and synophrys.

  7. Acro-oto-radial syndrome - Wikipedia

    en.wikipedia.org/wiki/Acro-oto-radial_syndrome

    Acro-oto-radial syndrome, also known as Pseudopapilledema blepharophimosis hand anomalies syndrome is a very rare hereditary disorder which is characterized by pseudopapilledema, hearing loss, cranio-facial dysmorphisms and hand/foot anomalies. [1] Unlike other genetic syndromes, people with this syndrome don't exhibit intellectual disabilities ...

  8. Young–Simpson syndrome - Wikipedia

    en.wikipedia.org/wiki/Young–Simpson_syndrome

    Diagnosis of Ohdo syndrome, SBBYS variant, is often confused with genitopatellar syndrome due to overlapping signs and symptoms. However, mask-like faces, blepharophimosis, and ptosis are symptoms that allow Ohdo syndrome, SBBYS variant, to be distinguished from genitopatellar syndrome.

  9. Ankyloblepharon - Wikipedia

    en.wikipedia.org/wiki/Ankyloblepharon

    Ankyloblepharon is a medical condition, defined as the adhesion of the edges of the upper eyelid with the lower eyelid. Ankyloblepharon must be differentiated from blepharophimosis, in which palpebral aperture is reduced and there is telecanthus, but the eyelid margins are normal.