Create issue ticket

51 Possible Causes for Cataracts Usually Congenital, Congenital Eye Anomaly, Saddle Nose

  • Congenital Syphilis

    Untreated early syphilis infections results in a high risk of poor pregnancy outcomes, including saddle nose, lower extremity abnormalities, miscarriages, premature births[en.wikipedia.org] Progression of untreated congenital syphilis can result in meningitis, hydrocephalus, and cranial nerve injuries. Chorioretinitis and cataracts may develop.[clinicaladvisor.com] nose and scars at the angles of the mouth.[medical-dictionary.thefreedictionary.com]

  • Congenital Malformation

    Four types of congenital cataracts, such as anterior polar, lamellar, polymorphic and total Red stethoscope and heart shape with plaster on it.[shutterstock.com] 740 Anencephalus and similar anomalies 741 Spina bifida 742 Other congenital anomalies of nervous system 743 Congenital anomalies of eye 744 Congenital anomalies of ear face[icd9data.com] Table 4 Frequency (and percentage of the total) of malformations by affected organ systems in subjects with multiple congenital anomalies.[bmcoralhealth.biomedcentral.com]

  • Late Congenital Syphilis

    The saddle nose deformity was due to the failure of development of nasal bones.[ijstd.org] Progression of untreated congenital syphilis can result in meningitis, hydrocephalus, and cranial nerve injuries. Chorioretinitis and cataracts may develop.[clinicaladvisor.com] Clinical examination showed the "saddle-nose" deformity, Hutchinson's teeth, high-arched palate, Dubois little-finger sign, and small maxillae resulting in shallow depression[ncbi.nlm.nih.gov]

  • Oculocerebrorenal Syndrome

    The hallmark of this disorder is the appearance of congenital bilateral cataracts (thick clouding of the lenses) that are usually deemed visually significant at birth.[news-medical.net] The classical diagnostic triad includes: Congenital cataracts Neonatal or infantile hypotonia with subsequent mental impairment Renal tubular dysfunction progressing to chronic[patient.info] The diagnosis is initially suggested by uniformly present congenital cataract, while the recognition of cerebral manifestations is based on a comprehensive neurological examination[news-medical.net]

  • Stickler Syndrome

    She also had micrognathia and a saddle nose, leading to a diagnosis of Stickler syndrome type 1.[ncbi.nlm.nih.gov] Abnormalities of vitreous gel architecture are a pathognomonic feature, usually associated with high myopia which is congenital and non-progressive.[ncbi.nlm.nih.gov] The vitreous showed distinct abnormalities consistent with congenital vitreous anomaly of type 1 Stickler syndrome.[ncbi.nlm.nih.gov]

  • Axenfeld-Rieger Syndrome Type 3

    Mortality/Morbidity Medical treatment usually fails in secondary congenital glaucoma, and surgery is necessary in most cases.[emedicine.medscape.com] Anomalies include anterior segment dysgenesis of the eye, dental anomalies, maxillary hypoplasia, periumbilical anomalies, and congenital heart defects.[karger.com] Axenfeld-Rieger syndrome (ARS) represents a spectrum of diseases that involve congenital anomalies of the anterior segment of the eyes.[genedx.com]

  • Congenital Cystic Eyeball

    Systemic associations [ 8 ] include saddle nose, facial clefting, nostril malformation, choanal atresia, malformation of the sphenoid bone and other neurological abnormalities[bmcophthalmol.biomedcentral.com] Microphthalmos - small eye without normal function (eg, cataract, coloboma, congenital cyst).[patient.info] […] of lacrimal gland 743.65 Specified congenital anomalies of lacrimal passages 743.66 Specified congenital anomalies of orbit 743.69 Other congenital anomalies of eyelids,[healthprovidersdata.com]

  • Autosomal Dominant Chondrodysplasia Punctata

    The disorder recognized by Hünermann also included micromelia, a saddle nose deformity, flexion contractures, cataracts, and a dermopathy.[mhmedical.com] Congenital ichthyosiform erythroderma. Alopecia of the scalp. Cataracts. Chondrodysplasia punctata, tibial-metaphyseal type – mesomelic type.[fetalultrasound.com] Family history was uneventful for genetic diseases, skeletal abnormalities, congenital anomalies and hearing loss.[molecularcytogenetics.biomedcentral.com]

  • Alagille Syndrome

    nose, and a small chin (Fig 1).[jamanetwork.com] , congenital deafness, neurosensory nephropathy Comment Alport syndrome is characterized by haematuric nephropathy, in most cases leading to renal failure (usually progressive[doi.org] 2006;79:169 ) Clinical features Reported incidence is 1:30,000 of live births Common clinical features: abnormal inverted triangular facies, posterior embryotoxon in the eye[pathologyoutlines.com]

  • Hunermann Conradi Syndrome

    The disorder recognized by Hünermann also included micromelia, a saddle nose deformity, flexion contractures, cataracts, and a dermopathy.[mhmedical.com] […] and cataracts.[dermatologyadvisor.com] […] cataracts and other eye abnormalities Developmental assessment (after the newborn period) Echocardiogram for possible congenital heart defect at the time of diagnosis Renal[ncbi.nlm.nih.gov]

Similar symptoms