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16 Possible Causes for Cataract, Mild Maxillary Prognathism

  • Peters Anomaly

    Hereditary congenital cataract is a well recognized but heterogeneous group of disorders; the cataracts may occur alone, or with other ocular or systemic abnormalities, and[ncbi.nlm.nih.gov] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] Use of an image-guided femtosecond laser for cataract extraction in Peters anomaly type 2 is a safe method for removing these complex cataracts while preserving capsular and[ncbi.nlm.nih.gov]

  • Rieger Syndrome

    To describe ultrasound biomicroscopy (UBM) features in a patient with Axenfeld-Rieger syndrome (ARS) and cataract before and after anterior segment surgery using intraocular[ncbi.nlm.nih.gov] Facies: - Maxillary hypoplasia - Mild prognathism ... Teeth: - Microdontia - Hypodontia - Cone - shaped teeth ... Ear: - Abnormal ear ... Abdomen: - Umbilical hernia ...[ibis-birthdefects.org] To our knowledge no case of congenital cataract with associated AxenfeldRieger anomaly is reported, so this is probably the first case report.[ophthalmologypakistan.com]

  • Axenfeld-Rieger Syndrome Type 3

    Brunescent cataract. The patient underwent cataract surgery OD.[webeye.ophth.uiowa.edu] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] Featured surgeries include: plastics, glaucoma, intraocular contact lens refractive, strabismus, and various techniques of cataract/IOL implantation.[books.google.com]

  • Craniosynostosis Type 3

    […] on chromosome 14q23 – MCOPCT3 (MIM 302300): incorporated into Cataract 40 (MIM 302200 ). – MCOPCT4 (MIM 610426), incorporated into Cataract 23 (MIM 610425 ): caused by mutation[bredagenetics.com] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] Red reflex testing should be performed to check for congenital cataracts.[patient.info]

  • 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] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] If the onset or distribution of poikiloderma is atypical, then two additional features such as bone abnormalities, cataracts, or osteosarcoma are required for a diagnosis[ncbi.nlm.nih.gov]

  • Hunermann Conradi Syndrome

    Short stature in combination with ichthyosis or alopecia, cataracts, and limb shortening in an adult should prompt consideration of a diagnosis of CDPX2.[jhu.pure.elsevier.com] She was determined to mandibular prognathism with mild mandibular shift to the left, maxillary deficiency, and potential involvement with a syndrome.[cyberleninka.org] In addition, treatment for cataracts is also recommended, either by surgically removing the cataracts or using corrective lenses, to help patients maintain good vision, and[patientworthy.com]

  • Peters Anomaly - Cataract Syndrome

    […] was reported in a family with microcornea, cataract syndrome.[ajol.info] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] […] types 1-6, 9-12, 14-18, 20-22, 33, 40 cataract, syndromic 11 cataract 13 with adult i phenotype cataract with late-onset corneal dystrophy congenital cataracts, facial dysmorphism[invitae.com]

  • Micrognathism

    Clinics: microcephaly, receding forehead. microphtalmia/anophtalmia, colobomata of the iris, cataract. arrhinencephaly, probocis. hypotelorism. scalp defect (in relation with[labmed.hallym.ac.kr] […] of the teeth -Mild prognathism www.indiandentalacademy.com 19.  Hypoparathyroidism - retarded eruption -early exfoliation -enamel defects  Hyperparathyroidism - demineralization[slideshare.net] […] philtrum (rare); Prognathism; [Ears]; Protruding ears; Cupped ears; Large ears; Dysplastic ears; Hearing loss (rare); [Eyes]; Upslanting palpebral fissures; Epicanthus; Cataract[findzebra.com]

  • Isolated Trigonocephaly

    […] intoxication (空) 【空回腸炎】*jejunoileitis 【空腸炎】*jejunitis 【空洞状脊髄脱出】*syringomyelocele 【空腹低血糖[症]】*fasting hypoglycemia 【空胞細胞症】*koilocytosis ( コイロサイトーシス) (楔) 【楔状白内障】*cuneiform cataract[medo.jp] Note maxillary hypoplasia, ocular proptosis with mild relative prognathism. (From Renier et al. 2000) syndrome is genetically heterogeneous.[rrnursingschool.biz] […] paralysis 【痙攣】*spasm *[ 全身痙攣] convulsion ( 攣縮) 【痙攣性狭窄】*spasmodic stricture 【痙攣性疾患】*convulsive disorder 【痙攣性喘息】*spasmodic asthma 【痙攣性大腸炎】*spastic colitis 【痙攣性白内障】*tetanic cataract[medo.jp]

  • Congenital Ectropion Uveae

    Central corneal pannus, cataract, foveal hypoplasia, decreased vision and nystagmus can be an association of aniridia.[ophthalmologypakistan.com] They include mild dysmorphism (hypertelorism, broad flat nose, maxillary hypoplasia, and mild prognathism), dental anomalies (microdontia, hypodontia, anodontia, oligodontia[glaucomatoday.com] […] uveae, and cataracts (Cheong et al. 2016.[preventiongenetics.com]

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