Conditions related to the eye?
Any eye injury?
Acanthamoeba Keratitis (Medical Emergency)
Ataxia (awkward eye-hand co-ordination, retinitis pigmentosa)
Ataxia with vitamin E deficiency (AVED) (retinitis pigmentosa)
Retinal Tear and Detachment (Medical Emergency)
Liver disease (Medical Emergency)
Age related degeneration
Acromegaly
Amyloidosis
Amenorrhea
Aniridia
Arcus Senilis
Astigmatism
Bell’s palsy (Facial palsy)
Blepharitis
Blocked tear ducts
Blood vessels in the eye that appear of bronze or grey colour?
Cataracts
Cogan type ocular motor apraxia (when eyes move side to side and then shake head)
Coloboma
Congenital type 1 plasminogen deficiency (growths of wooden appearance in and around eyes)
Danon disease (Glycogen storage disease)
Diabetic retinopathy
Diplopia (double vision)
Ectropion
Entropion (Trichiasis)
Episcleritis [inflammation in the episclera of the eye – the episclera is the tissue that lies over the sclera (the white of the eye)]
Erdheim-Chester disease
Erythema nodosum
Exposed to Ultra-violet light
Folic acid deficiency (anaemia)
Glaucoma
Goldenhar disease (which affects eye, ear, and spine development)
Hemianopia (where there is a loss of one half of your visual field – caused by damage to the brain, for example, by a stroke, trauma or tumour. The extent of field loss can vary and depends of the area of your brain that has been affected)
Hyperopia (Long-sightedness)
Hyperthyroidism (Grave’s Disease)
Hypothyroidism
Hyperoxaluria and Oxalosis
Iron deficiency
Klumpke’s palsy (Dejerine-Klumpke palsy)
Keratitis
Kerataconus
Krabbe disease
Lazy eye (amblyopia)
Leber congenital amaurosis (common inherited eye disorder at birth)
Leber’s disease
Lysosomal Lipid Storage and/or Lysosomal Lipid Metabolism Disorders and/or Mucopolysaccharides Metabolism Disorders (Mucopolysaccharidoses)
Lyme disease
Lupus
Macular degeneration
Meibomian cyst
Microphthalmia
Mitochondrial Myopathy and/or Encephalomyopathy
Mucormycosis (Medical Emergency)
Myopia (Short-sightedness)
Non-Hodgkin’s lymphoma
Nystagmus
Ocular albinism type I (male)
Ocular albinism with late onset sensorineural deafness (blue eyes and late deafness)
Oculo-auriculo-vertebral spectrum [abnormalities tend to involve the cheekbones, jaw, mouth, ears, eyes, and/or bones of the spinal column (vertebrae)]
Orbital Myositis (idiopathic orbital or Ocular myositis)
Polycythaemia vera
Presbyopia
Progeria disease
Pterygium and/or Pinguecula
Refsum Disease (Zellweger spectrum disorders)
Retinitis Pigmentosa (common inherited eye disorder noticeable between birth years until 40 years of age)
Retinoblastoma (eye cancer)
Sarcoidosis
Scratched eye
Sialidosis (cherry red spots in the eyes)
Squint (strabismus)
Surgery and/or laser treatment in last 6 months
Tardive dyskinesia
Thyroid eye disease or Graves’ ophthalmopathy
Tunnel vision [loss of peripheral (outer) vision with retention of central vision]
Eye Ulcer
Uveitis
Reduced visual acuity
Visual field defect
Wegener’s Granulomatosis
Wernicke encephalopathy
Wilson disease
Xanthelasmata (high cholesterol)
X-linked retinoschisis (males only)
Reactive arthritis
Sickle cell disease
Visual snow (tiny flickering dots that resemble the noise of a detuned analogue television)
Vitamin B12 Deficiency (Anaemia)
Xeroderma Pigmentosum
Other:
Syndromes related to the eye?
Acrocephalopolysyndactyly disorders (Apert syndrome, Pfeiffer syndrome, Chotzen syndrome, Carpenter syndrome)
Adie syndrome (Holmes-Adie syndrome)
Alport Syndrome
Alström syndrome
Angelman syndrome
Antiphospholipid/Hughes syndrome (Affect brain, respiratory, kidney, skin)
Behcet syndrome
Boerhaave Syndrome (Medical Emergency)
Coffin-Siris syndrome
Cogan’s syndrome
Cornelia de Lange syndrome
Corneal erosion syndrome
De Barsy syndrome (eyes, loose saggy skin, weak muscles)
Xeroderma Pigmentosum (De Sanctis-Cacchione syndrome) (blistering of skin)
DiGeorge syndrome
Dry Eye Syndrome (Keratoconjunctivitis)
Dubowitz syndrome (narrow or triangle-shaped face with a high or sloping forehead, eczema, vision problems)
Guillian-Barre Syndrome (Weak and numb arms , legs and body, usually after a chest infection) (Medical Emergency)
Gustavson syndrome
Horner syndrome
Human HOXA1 syndromes (Athabaskan Native Americans, Middle East)
Joubert syndrome [lack of muscle control (ataxia), abnormal breathing patterns (hyperpnea), sleep apnoea, abnormal eye and tongue movements and low muscle tone]
Kabuki syndrome
Kearns-Sayre Syndrome
Klippel-Feil syndrome
Korsakoff Syndrome
Lacrimo-auriculo-dento-digital (LADD) syndrome (dry eyes, mouth , finger deformities)
Lymphedema-distichiasis syndrome (extra eye lashes with leg swelling)
Marfan syndrome
Moebius Syndrome
Nail Patella syndrome [Lester’s sign- abnormally dark (hyperpigmented) and “cloverleaf” shape discoloration around the inner margin (pupillary margin) of the coloured portion of the eyes]
Nelson syndrome – [one to four years following the surgical removal of the adrenal glands (bilateral adrenalectomy)]
Parinaud Syndrome
Prader-Willi syndrome
Congenital Rubella Syndrome
Rubinstein-Taybi syndrome
Schwartz-Jampel Syndrome/Stuve-Wiedemann Syndrome
Senior-Løken syndrome (vision loss and kidney failure)
Serotonin Syndrome
Smith Lemli Opitz syndrome
Sotos syndrome
Toxic Shock Syndrome (occur after an infection and/or use of tampons)
Tumor Necrosis Factor Receptor Associated Periodic Syndrome
Usher syndrome (rare genetic disease that affects both hearing and vision)
Wallenberg syndrome
Weill Marchesani syndrome [short stature, broad head (brachycephaly) and joint stiffness]
Wolfram syndrome
Wolf-Hirschhorn syndrome
Wyburn-Mason syndrome [eyes bulge forward (proptosis), drooping of the upper eyelid (blepharoptosis), difficulty moving the eyes (ocular motility disorders)]
Other: