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15 Possible Causes for Cataract, Prominent High Nasal Root, Retinopathy of Prematurity

  • Congenital Cataract

    Note that cataract may affect one or both eyes.[symptoma.com] We present a Hungarian girl with microcephaly, microphthalmia, congenital cataract, prominent nasal root, peaked nose, micrognathia with high arched palate, mild mental retardation[ncbi.nlm.nih.gov] Ive been thinking about doing another one for quite and I figured… Read More We are excited to announce our newest awareness shirt for ROP (Retinopathy of prematurity).[eyepowerkidswear.com]

  • Malignant Hyperthermia - Arthrogryposis - Torticollis

    […] disease (略 COLD) 【慢性副鼻腔炎】*chronic paranasal sinusitis 【慢性リンパ性白血病】*chronic lymphocytic leukemia (略 CLL) (味) 【味覚過敏】【味覚亢進】*gustatory hyperesthesia *hypergeusia (未) 【未熟児網膜症】*retinopathy[medo.jp] […] complementation type Methylenetetrahydrofolate reductase deficiency Methylmalonic acidemia with homocystinuria Methylmalonic acidemia Methylmalonic aciduria microcephaly cataract[en.wikipedia.org] […] of the zygomatic bone Prominence of cheekbone Pronounced cheekbone [ more ] 0012370 Prominent nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose[rarediseases.info.nih.gov]

  • Microcephalic Osteodysplastic Primordial Dwarfism Type II

    […] of prematurity; 133780; FZD4 Rett syndrome; 312750; MECP2 Rett syndrome, congenital variant; 613454; FOXG1B Rett syndrome, preserved speech variant; 312750; MECP2 Revesz[howlingpixel.com] nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Proximal[rarediseases.info.nih.gov] Reynolds, An apparently new syndrome of microcephalic primordial dwarfism and cataracts, American Journal of Medical Genetics, 25, 1, (1-8), (2005). R. M. Winter, J.[doi.org]

  • Myopia Type 15

    Refractive errors and strabismus in premature Asian infrants with and without retinopathy of prematurity. Singapore Med J 2000;41(8):393–397. PubMed Google Scholar 61.[link.springer.com] SYNDROME Cataract, microcornea, microphakia, keratoconus, glaucoma, ptosis AD LMX1B #161200 NANCE-HORAN SYNDROME Congenital cataracts, glaucoma, microphthalmia, microcornea[eyewiki.aao.org] […] frontal bossing, thick eyebrows, prominent nasal root and tip high arched palate, micrognathia, smooth and silky skin, especially at the trunk, elastic skin at the knees,[omicsonline.org]

  • Baller-Gerold Syndrome

    Complications include a high risk of skin cancer, with about half having skin cancer by age 10 without preventive efforts, and cataracts.[howlingpixel.com] nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Scoliosis[rarediseases.info.nih.gov] […] of Prematurity Stages III, IV Rett syndrome Rickets Rieger syndrome Roberts SC Phocomelia Robinow syndrome 15.[de.slideshare.net]

  • Ectrodactyly

    These findings were absent in our case, that had only a retinopathy associated to the prematurity.[scielo.br] Additional abnormalities such as alopecia, cataract, absent eyebrows, and oligodontia may occur.[ncbi.nlm.nih.gov] Reported dysmorphisms include high forehead, prominent eyes, long eyelashes, hypertelorism, flat nasal root, low-set dysmorphic ears (figure 1A, B, D ).[ojrd.biomedcentral.com]

  • Myopia Type 22

    No participant had any known ocular disease or insult that could predispose to myopia, such as a history of retinopathy of premature or neonatal problems, or a known genetic[molvis.org] This richly illustrated, full color text covers areas such as: malformations; refractive errors, the cornea, glaucoma and cataracts; retina and the optic nerve; eye movement[books.google.com] […] frontal bossing, thick eyebrows, prominent nasal root and tip high arched palate, micrognathia, smooth and silky skin, especially at the trunk, elastic skin at the knees,[omicsonline.org]

  • Congenital Disorder of Glycosylation Type 1Q

    Both of our patients have severe visual impairment, optic atrophy, and cataracts.[bmcmedgenet.biomedcentral.com] […] bridge ; Prominent, high and nasal root; Tubular nose; [Mouth]; Thin upper lip; Drooling; [Teeth]; Crowded teeth ABDOMEN: [Gastrointestinal]; Chewing abnormalities GENITOURINARY[findzebra.com] 8.6**903 Von Willebrand disease 12.5 3280 Syringomyelia 8.570482 Esophageal carcinoma 12.5 644 NARP syndrome 8.490050 Retinopathy of prematurity 12.2* 90290 CREST syndrome[fliphtml5.com]

  • MORM Syndrome

    prematurity; and minimally invasive strabismus surgery.[books.google.de] Showing of 9 Percent of people who have these symptoms is not available through HPO Autosomal recessive inheritance 0000007 Cataract Clouding of the lens of the eye Cloudy[rarediseases.info.nih.gov] nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Reduced[rarediseases.info.nih.gov]

  • Ocular Albinism with Congenital Sensorineural Deafness

    Dysphagia Gait disturbance Axonal loss Decreased nerve conduction velocity Hyperreflexia Impaired vibratory sensation Nyctalopia Abnormality of retinal pigmentation Pigmentary retinopathy[mendelian.co] Deafness Clinical Characteristics Ocular Features: A 5 year old male has been described with uveal colobomas in microphthalmic eyes plus small corneas with a pannus, dense cataracts[disorders.eyes.arizona.edu] nasal root, prominent columella Hypoplastic alae nasi Premature gray hair (age Type I Waardenburg syndrome is characterized by evidence of dystopia canthorum and the full[centogene.com]

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