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Rare eyelid malformation
- ... TUBB2B gene has been found to cause a rare form of congenital fibrosis of the ... a brain malformation called polymicrogyria, in which the surface of the ...
- ... symptoms. Both types I and II include the eyelid malformations and other facial features. Type I is also ... as various activities in the ovaries, resulting in eyelid malformation and abnormally accelerated maturation of certain ovarian cells ...
- ... eye that produce and secrete tears. Lacrimal system malformations that can occur with LADD syndrome include an underdeveloped or absent opening to the tear duct at the edge of the eyelid (lacrimal puncta) and blockage of the channel (nasolacrimal ...
- Hemangioma (American Academy of Orthopaedic Surgeons)Benign Tumors/Specifics ... Benign Tumors ... Vascular Diseases/Specifics ... Vascular Diseases ... American Academy of Orthopaedic Surgeons ... A hemangioma is a noncancerous ...
- ... 4 (SHFM4), a condition involving hand and foot malformations without any other signs or symptoms. Additionally, TP63 gene mutations are a rare cause of cleft lip and/or cleft palate ...
- ... or complete fusion of the upper and lower eyelids, the bottom of the tongue attached to the floor of the mouth, or a small lower jaw (micrognathia). Tetra-amelia syndrome is a very rare condition that has been described in only a ...
- ... with port-wine stains involving upper and lower eyelids Neurologic problems when port-wine stain is associated with a disorder such as Sturge-Weber syndrome
- ... result, the person may have double vision and eyelid drooping. ... birth (congenital) Increased brain pressure (brain herniation) In ... with diabetes may also develop a neuropathy of the third nerve .
- ... the condition called CFEOM3, and they are a rare cause of another form called ... have droopy eyelids (ptosis). In addition, people with CFEOM3 can have ...
- ... skin disorder called eczema. Some affected individuals have malformations of the brain, heart, gastrointestinal system, kidneys, or genitalia. A few people with 2q37 deletion syndrome develop a rare form of kidney cancer called Wilms tumor. 2q37 ...