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4,962 Possible Causes for Cataract, Prominent High Nasal Root, Umbilical Plaque

  • Schwartz-Jampel Syndrome

    Ocular manifestation is a part of the syndrome and include blepharospasm, cataract, subluxation of lens and myopia.[ajol.info] nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Ptosis[rarediseases.info.nih.gov] […] developmental, eye, genetic, neurological Phenotypes Abnormality of femoral epiphysis ; Anterior bowing of long bones ; Autosomal recessive inheritance ; Blepharophimosis ; Cataract[mousephenotype.org]

  • Kniest Dysplasia

    The cataract could also develop as a posteriorcapsular opacity and progress to a total cataract.[jamanetwork.com] Dislocated lens, cataract, and vitreoretinal degeneration can also be encountered.[symptoma.com] Femoral capital epiphyses and the presence of a cataract in one eye were noted from the early stages of the patient's life. The patient's final height was 165 cm.[ncbi.nlm.nih.gov]

    Missing: Prominent High Nasal Root
  • Smith Lemli Opitz Syndrome

    These postnatal cataracts appear to be due to a different pathological mechanism and have a different clinical course than the typical congenital cataracts that occur in SLOS[ncbi.nlm.nih.gov] […] retinal abnormalities may be noted on electroretinography. [18] Cataracts may occur acutely in the postnatal period. [19] Hearing loss is fairly common.[emedicine.medscape.com] We report on two patients with severe Smith-Lemli-Opitz syndrome who acutely developed postnatal cataracts.[ncbi.nlm.nih.gov]

    Missing: Prominent High Nasal Root
  • Patau Syndrome

    Heart defects Structural eye defects, including microphthalmia, Peters anomaly, cataract, iris and/or fundus (coloboma), retinal dysplasia or retinal detachment, sensory nystagmus[cytogenx.com] Agenesia (complete) absence of the corpus callosum enlarged cisterna magna Eye malformations: Coloboma : Gap formation of the iris, lense or choroid Retinaal abnormalities Cataract[flexikon.doccheck.com] Structural eye defects, including microphthalmia, Peters' anomaly, cataract, iris or fundus (coloboma), retinal dysplasia or retinal detachment, sensory nystagmus, cortical[en.wikipedia.org]

    Missing: Prominent High Nasal Root
  • Endometriosis

    24·2 to 26·4) * 0·6 ( 0·0 to 1·3) Glaucoma 5954·5 (5077·5 to 6905·8) 39·1 (36·9 to 41·4) * 4·2 (2·8 to 5·5) * 541·3 (370·0–747·9) 39·4 (37·0 to 41·9) * 4·3 (2·6 to 5·8) * Cataract[ncbi.nlm.nih.gov]

    Missing: Prominent High Nasal Root
  • Hallermann-Streiff Syndrome

    To report two cases of Hallermann-Streiff syndrome with exudative retinal detachment after cataract surgery. Case report.[ncbi.nlm.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 Pulmonary[rarediseases.info.nih.gov] Ophthalmic abnormalities included bilateral congenital cataract. Glaucoma is uncommon.[ncbi.nlm.nih.gov]

    Missing: Umbilical Plaque
  • Lytic Bone Lesion

    […] disorder / nasal speech - Aortic valve atresia / stenosis / narrowing / supra-aortic / supra-valvular stenosis - Bowed diaphysis / diaphyses / long bones - Broad nasal root - Cataract[csbg.cnb.csic.es] Ablepharon macrostomia syndrome Abnormal systemic venous return Abruzzo Erickson syndrome Absence of Gluteal muscle Absence of tibia with polydactyly Absent corpus callosum cataract[wikidoc.org] […] macrostomia syndrome Ablutophobia Abnormal systemic venous return Abruzzo Erickson syndrome Absence of Gluteal muscle Absence of tibia with polydactyly Absent corpus callosum cataract[starrepublic.org]

    Missing: Prominent High Nasal Root
  • 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] From Wikidata Jump to navigation Jump to search disorder of lens edit Language Label Description Also known as English Congenital cataract disorder of lens Statements subclass[wikidata.org]

    Missing: Umbilical Plaque
  • Chudley-Rozdilsky Syndrome

    Microcornea Syndrome Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome Cataracts, Ataxia, Short Stature, and Mental Retardation Catel Manzke Syndrome Cauda equina[rgd.mcw.edu] nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Protruding[rarediseases.info.nih.gov] Muscular dystrophy, congenital, infantile with cataract and hypogonadism 0 *Cataract *Hypogonadism *Muscular Dystrophies/congenital.[reference.md]

    Missing: Umbilical Plaque
  • Hypertrichotic Osteochondrodysplasia

    , see hyperferritinemia-cataract syndrome hereditary hyperferritinemia-cataract syndrome , see hyperferritinemia-cataract syndrome hereditary hyperparathyroidism-jaw tumor[herenciageneticayenfermedad.blogspot.com] […] syndrome Cataract-hypertrichosis-intellectual disability syndrome Cataract-intellectual disability-anal atresia-urinary defects syndrome Cataract-intellectual disability-hypogonadism[se-atlas.de] […] glycosylphosphatidylinositol deficiency 2 Families 163985 Hyperekplexia-epilepsy syndrome 2 Cases 168956 Hypereosinophilic syndrome 1.5 P * 2410 Hypergonadotropic hypogonadism-cataract[azkurs.org]

    Missing: Prominent High Nasal Root

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