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94 Possible Causes for Cataracts Usually Congenital, Congenital Eye Anomaly, Thin Lips

  • Hallermann-Streiff Syndrome

    […] bilateral congenital cataracts, and microphthalmia.[profiles.uchicago.edu] Hallermann-Streiff syndrome is a rare congenital disorder characterized as a complex association of developmental anomalies involving structures of ectodermal origin (the[ncbi.nlm.nih.gov] […] calvarium Thin cranial bone 0010539 Thin ribs Slender ribs 0000883 Thin vermilion border Decreased volume of lip Thin lips [ more ] 0000233 Wormian bones Extra bones within[rarediseases.info.nih.gov]

  • Congenital Cataract

    What percentage of congenital cataracts are inherited and part of syndromes? Bilateral congenital cataracts are usually inherited or acquired?[quizlet.com] The mouth is small and the upper lip is thin. The scalp hair may be sparse and the nails sometimes appear dystrophic.[disorders.eyes.arizona.edu] Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 5 Walker-Warburg Syndrome Or Muscle-Eye-Brain Disease, FKRP-Related MDDGA5 613153[ukgtn.nhs.uk]

  • Autosomal Dominant Mental Retardation Type 21

    Cataracts, Congenital, with Cleft Palate Clinical Characteristics Ocular Features: Bilateral congenital cataracts are usually present together with upward-slanting and narrowed[disorders.eyes.arizona.edu] lips.[content.sciendo.com] […] with brain and eye anomalies), type a, 8 C3553813 OMIM933HP:0001263 HP:0001263 Global developmental delay0 POMK 84197 615249 Muscular dystrophy-dystroglycanopathy (congenital[mseqdr.org]

  • Lens Coloboma

    […] and Associated Systemic Diseases (see: Systemic Diseases) Congenital and Juvenile Cataracts, Usually Bilateral (see also: Congenital Syndromes) Anterior and Posterior Lenticonus[atlasophthalmology.net] Lens colobomas are congenital lens anomaly, rarely seen with Marfan syndrome. They are usually managed conservatively.[ncbi.nlm.nih.gov] […] upper lip and flattening of the maxillary ‎ Seite 88 - JK et al. (1982) Ethanol-associated selective fetal malnutrition.[books.google.de]

  • Peters Anomaly

    A family is described in which congenital cataracts with microcornea, and Peters' anomaly, appear to be variable expressions of a generalized anterior segment disorder inherited[ncbi.nlm.nih.gov] Category Congenital malformation Brite Human diseases [BR: br08402 ] Congenital malformations Congenital malformations of eye H01075 Peters anomaly Human diseases in ICD-11[genome.jp] With the presence of clinical features such as bilateral Peters' anomaly, short stature, cleft lip and palate, typical facial features (thin upper lip, round face, low set[jcnonweb.com]

  • Isolated Congenital Sclerocornea

    […] is one of the most serious complications occurring after infantile cataract surgery for congenital idiopathic cataract, cataract associated with ocular or systemic syndromes[dovepress.com] A congenital anomaly in which the whole or part of the cornea is opaque and resembles the sclera; other ocular abnormalities are frequently present. sclerocornea /scle·ro·[medical-dictionary.thefreedictionary.com] lips and micrognathia), and mild to moderate intellectual deficiency.[mendelian.co]

  • Kaufman Oculocerebrofacial Syndrome

    Electroretinogram (ERG) responses are usually nonrecordable.[mendelian.co] […] eyebrow Thin eyebrows 0045074 Thin vermilion border Decreased volume of lip Thin lips [ more ] 0000233 Wide mouth Broad mouth Large mouth [ more ] 0000154 5%-29% of people[rarediseases.info.nih.gov] anomaly characterized by abnormal smallness of one or both eyes.[rarediseases.oscar.ncsu.edu]

  • Microphthalmos

    Other congenital diseases such as microcornea , microcoria , heterochromia iridis , microlentia , cataracts , retinal dysplasia , retinal detachment , anterior segment dysgenesis[vetbook.org] Our case presented with thinning of the corpus callosum and mild mental retardation, besides cleft lip and palate.[ijri.org] Four children with severe congenital eye anomalies are described of which three had related symptoms.[ncbi.nlm.nih.gov]

  • Rieger Syndrome

    Microphthalmos - small eye without normal function (eg, cataract, coloboma, congenital cyst).[patient.info] Deletion mapping indicates that psychomotor retardation, coloboma, prominent forehead, epicanthus, broad based nose, and broad, thin upper lip are associated with monosomy[ncbi.nlm.nih.gov] Q13.4 Other congenital corneal malformations Q13.8 Other congenital malformations of anterior segment of eye Q13.81 Rieger's anomaly Q13.89 Other congenital malformations[icd10data.com]

  • Eye Muscle Disorder

    In some people, the condition can also cause cataracts to develop at a younger age than usual. Life expectancy for people with myotonic dystrophy can vary considerably.[nhs.uk] Cornelia deLange Syndrome Typical facial features include thin eyebrows that meet in the middle, long eyelashes, a short upturned nose, and thin downturned lips.[apraxia-kids.org] : Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies; Congenital muscular dystrophy due to dystroglycanopathy Muscle eye brain disease (MEB) belongs[rarediseases.info.nih.gov]