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Cat-eye syndrome (CES) or Schmid–Fraccaro syndrome is a rare condition caused by an abnormal extra chromosome, i.e. a small supernumerary marker chromosome. [2] This chromosome consists of the entire short arm and a small section of the long arm of chromosome 22 .
Symptoms of pterygium include persistent redness, [9] inflammation, [10] foreign body sensation, tearing, dry and itchy eyes. In advanced cases the pterygium can affect vision [ 10 ] as it invades the cornea with the potential of obscuring the optical center of the cornea and inducing astigmatism and corneal scarring. [ 11 ]
Dry eye syndrome, also known as keratoconjunctivitis sicca, is the condition of having dry eyes. [2] Symptoms include dryness in the eye, irritation, redness, discharge, blurred vision, and easily fatigued eyes. Symptoms range from mild and occasional to severe and continuous. [3]
Furthermore, the lack of tissue in Caitin's eye gives her a "cat-like" look. See more photos of Caitin: It is believed that only 1 out of 150,000 people are diagnosed with the syndrome.
Popliteal pterygium syndrome, a congenital condition affecting the face, limbs, or genitalia but named after the wing-like structural anomaly behind the knee. Pterygium (eye) or surfer's eye, a growth on the cornea of the eye. Pterygium colli or webbed neck, a congenital skin fold of the neck down to the shoulders.
Difference between pterygium and pseudopterygium Pterygium Pseudopterygium Etiology Degenerative process: Inflammatory process Age Common in adults [5] Occur in any age Site Horizontally, most commonly nasally [4] Anywhere Status Progressive(commonly) or stationary [5] Always stationary Neck Adherent to limbus [5] Free Probe test
The post Lentigo in Cats: Symptoms, Causes, & Treatments appeared first on CatTime. Lentigo in cats is a common dermatological condition characterized by the presence of small, flat, brownish ...
Bartsocas-Papas syndrome is a form of popliteal pterygium syndrome and is a very rare disease characterized by congenital craniofacial anomalies, popliteal webbing, and genitourinary and musculoskeletal anomalies. It was first described by Dr. Christos Bartsocas and is more specifically an autosomal recessive popliteal pterygium syndrome. [8]