Juvenile Cataract: Causes & Reasons

Possible Causes for Juvenile Cataract

Nearly 10-40% patients will develop bilateral juvenile cataract by 4-7 years of age and about 30% will have hypogonadism. [1] Nails may be dystrophic and hair (scalp, beard [idoj.in]

cataracts. [geneskin.org]

Recently we encountered a 25-year-old white woman who had developed this syndrome but without juvenile cataracts, hypogonadism, or mental retardation. [ncbi.nlm.nih.gov]

Werner Syndrome

Examination disclosed juvenile cataracts, scleroderma-like skin changes, hair loss, deficiency of adipose tissue, and sensory neuropathy of the lower limbs (right panel). [nejm.org]

Rothmund-Thomson syndrome is a rare autosomal dominant disorder characterized by photosensitivity, poikilodermatous skin changes, juvenile cataracts, skeletal dysplasia, and [ijdvl.com]

The patient had a high-pitched voice, hoarseness, a characteristic bird-like facial appearance with a beak-shaped nose, canities and juvenile cataracts. [ncbi.nlm.nih.gov]

Traumatic Cataract

H26 Other cataract Excludes1 congenital cataract ( Q12.0 ) H26.0 Infantile and juvenile cataract H26.00 Unspecified infantile and juvenile cataract H26.001 Unspecified infantile [icd10coded.com]

cataract H26.09 Other infantile and juvenile cataract H26.1 Traumatic cataract H26.10 Unspecified traumatic cataract H26.11 Localized traumatic opacities Reimbursement claims [icd10data.com]

[…] and Associated Systemic Diseases (see: Systemic Diseases) Congenital and Juvenile Cataracts, Usually Bilateral (see also: Congenital Syndromes) Intraocular Diseases, Cataracta [atlasophthalmology.net]

Congenital Cataract

Nine other families have been previously reported with dominant congenital/juvenile cataracts and mutations in EPHA2. [ncbi.nlm.nih.gov]

Childhood cataracts are often referred to as: congenital cataracts – cataracts present when a baby is born or shortly afterwards developmental, infantile or juvenile cataracts [nhs.uk]

These are known as childhood cataracts. [nhs.uk]

Congenital Malformation of the Eye

Page updated June 2018 *Congenital and juvenile cataracts. Ophthalmology, 3rd ed. 2008. **Pediatric cataracts. Textbook of Family Practice, 7th ed. 2007. [allaboutvision.com]

Medical and surgical management of glaucomas affecting infants and children such as congenital glaucoma, juvenile glaucoma, uveitic glaucoma, and traumatic glaucoma. [medicine.umich.edu]

Clinical Interests Medical and surgical management of congenital eye diseases such as cataracts, anterior segment dysgenesis, primary congenital glaucoma, aniridia, Peters [medicine.umich.edu]

Progeria

cataracts Hypogonadism Tendency to diabetes Calcification of the blood vessels FULL TEXT [annals.org]

[…] syndrome are: Shortness of stature, characteristic habitus Canities (i.e., premature graying of the hair) Premature baldness Scleropoikiloderma Trophic ulcers of the legs Juvenile [annals.org]

Myotonic Dystrophy

In contrast, earlier onset forms including congenital, infantile, and juvenile DM1 are associated with poor muscle tone. [guito.kunt1m.us]

[…] and (iv) congenital types: (i) mild DM1: mildly symptomatic patients may have premature cataracts and baldness as the sole clinical features. [nature.com]

[…] in congenital and juvenile-onset patients. ○ Recommend annual eye examination, including slit-lamp eye examination. ○ Advise patient on safety measures regarding adjusting [cp.neurology.org]

Coronary Cataract

[…] and Associated Systemic Diseases (see: Systemic Diseases) Congenital and Juvenile Cataracts, Usually Bilateral (see also: Congenital Syndromes) Anterior and Posterior Lenticonus [atlasophthalmology.net]

[…] in the periphery without relevance to vision Author(s): McCuen, Brooks, M.D., Duke University Eye Center, Durham, NC, USA ICD10-Code: H25.0 Path: Lens -> Congenital and Juvenile [atlasophthalmology.net]

Lens -> Congenital and Juvenile Cataracts, Usually Bilateral (see also: Congenital Syndromes) Coronary Cataract, Progressive variant thumbnails view legends view -------- [atlasophthalmology.net]

Fabry Disease

Fabry disease, also known as Anderson-Fabry disease, angiokeratoma corporis diffusum and alpha-galactosidase A deficiency, is a rare genetic lysosomal storage disorder. Some cases show no significant clinical manifestations. In other cases, the clinical manifestations of Fabrys disease appear early in life. With age,[…] [symptoma.com]

Turner Syndrome

Turner syndrome, first described in 1938 by Henry Turner, is as loss or abnormality of the second X chromosome in at least one cell line in a phenotypic female. At birth, girls with Turner syndrome may have swollen hands and feet because of lymphedema. The blend of dysplastic or hypoplastic nails and lymphedema[…] [symptoma.com]

Early-Onset Anterior Polar Cataract

[…] nuclear cataract H26.04 Anterior subcapsular polar infantile and juvenile cataract H26.049 …… unspecified eye H26.05 Posterior subcapsular polar infantile and juvenile cataract [icd10data.com]

cataract needle cataract needle cataract needle cataract needle cataract pulverulent juvenile-onset MAF-related cataract removal cataract spoon Cataract surgery Cataract surgery [acronyms.thefreedictionary.com]

Convert to ICD-10-CM : 366.01 converts approximately to: 2015/16 ICD-10-CM H26.049 Anterior subcapsular polar infantile and juvenile cataract, unspecified eye Approximate [icd9data.com]

Cerulean Cataract

Thanks http://www.icd10data.com/ICD10CM/Cod...9/H25-H28/H26- H26Other cataract H26.0Infantile and juvenile cataract H26.00Unspecified infantile and juvenile cataract H26.001â [aapc.com]

Lens -> Congenital and Juvenile Cataracts, Usually Bilateral (see also: Congenital Syndromes) Cataracta Cerulea (Blue Dot Cataract) Cataracta Coerulea and Anterior Stellate [atlasophthalmology.net]

Cerebrotendinous Xanthomatosis

Juvenile cataract morphology in 3 siblings not yet diagnosed with cerebrotendinous xanthomatosis. Ophthalmology. 2013;120:956–60. [ncbi.nlm.nih.gov]

Chronic diarrhea and juvenile cataracts: think Cerebrotendinous Xanthomatosis and treat. [ncbi.nlm.nih.gov]

The presentation may range from infantile-onset diarrhea, juvenile-onset cataracts, tendon xanthomas, and progressive neurologic impairments. [ncbi.nlm.nih.gov]

Laurence Moon Syndrome

Volume : IX, Issue : VII, July - 2019 Dr. Samreen Mehfooz, Dr. Neelima Mehrotra, Dr. Amrita Bajpai, Dr. Akhil Agarwal, Dr. Aishwarya Madharia, Dr. Manmeet Singh Abstract : METHODS : A 15 years old female was ought with chief complaints of diminution of vision both eyes since birth. On ocular examination patient had[…] [worldwidejournals.com]

Froehlich Syndrome

Clinical Neuropathology, Volume 26 - Sept/Oct (232 - 240) Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein S. Krause, T. Göhringer, M.C. Walter, B.G.H. Schoser, P. Reilich, J. Linn, G.E. Pöpperl, L. Frölich, F. Hentschel, H. Lochmüller, A. Danek 1[…] [dustri.com]

Cockayne Syndrome

The molecular basis of Cockayne Syndrome From 2011-01-01 to 2015-12-31, closed project Project details EU contribution: EUR 1 499 235 Coordinated in: Switzerland Funding scheme: ERC-SG - ERC Starting Grant Objective Cockayne syndrome is a congenital disease with impaired DNA repair in actively transcribed genes.[…] [cordis.europa.eu]

Galactosemia

Galactosemia: An inherited disorder of galactose metabolism that occurs in newborns and can result in damage to the liver, brain, kidneys, and other organs in infants due to the accumulation of galactose derivatives in the body. Individuals with galactosemia cannot tolerate any amount of human or animal milk intake.[…] [medicinenet.com]

Lecithin Acyltransferase Deficiency

Lecithin cholesterol acyltransferase deficiency ( LCAT deficiency ) is disorder of lipoprotein metabolism. [1] Lecithin cholesterol acyltransferase catalyzes the formation of cholesterol esters in lipoproteins. Types The disease has two forms: [2] familial LCAT deficiency in which there is complete LCAT deficiency. fish[…] [ipfs.io]

Congenital Rubella Syndrome

Corneal edema occurring in the congenital rubella syndrome can result from coexistent glaucoma or develop in the absence of an elevated intraocular pressure. We examined a 36-week-old female infant with documented congenital rubella syndrome who had bilateral corneal stromal edema without attendant congenital[…] [ncbi.nlm.nih.gov]

Anterior Polar Cataract

Convert to ICD-10-CM : 366.01 converts approximately to: 2015/16 ICD-10-CM H26.049 Anterior subcapsular polar infantile and juvenile cataract, unspecified eye Approximate [icd9data.com]

cataract, unspecified eye (approximate) ICD-9-CM Siblings (same level / similar specificity) of 366.01: 366.00 - Nonsenile cataract, unspecified 366.02 - Posterior subcapsular [emedcodes.com]

(OD, Colour Image) Lens -> Congenital and Juvenile Cataracts, Usually Bilateral (see also: Congenital Syndromes) -> Anterior and Posterior Polar Cataract Unilateral Congenital [atlasophthalmology.net]

Retinal Pigmentary Dystrophy

The syndrome consisted of hypotrichosis with the typical SEM (scanning electron microscopy) changes of uncombable hair, retinal pigmentary dystrophy, juvenile cataract, oligodontia [ncbi.nlm.nih.gov]

cataract 60 33 hallmark (90%) Very frequent (99-80%) HP:0001118 5 uncombable hair 60 33 hallmark (90%) Very frequent (99-80%) HP:0030056 6 increased number of teeth 60 33 [malacards.org]

cataract ; Microdontia ; Oligodontia ; Pili canaliculi ; Rod-cone dystrophy ; Short metacarpal ; Short proximal phalanx of finger ; Short toe ; Uncombable hair Associated [mousephenotype.org]

Lamellar Cataract

Synonyms Infantile and juvenile cataract Infantile and juvenile cortical, lamellar, or zonular cataract Lamellar zonular cataract ICD-9-CM Volume 2 Index entries containing [icd9data.com]

But, so far, just one paper has reported that a BFSP1 mutation causes autosomal recessive juvenile onset cataract [ 12 ]. [molvis.org]

More examples of cataracts associated with systemic conditions: Juvenille idiopathic arthritis Galactosemia-associated cataract [cataractcourse.com]

Tricho-Retino-Dento-Digital Syndrome

cataract 58 31 hallmark (90%) Very frequent (99-80%) HP:0001118 4 uncombable hair 58 31 hallmark (90%) Very frequent (99-80%) HP:0030056 5 sparse hair 31 hallmark (90%) HP [malacards.org]

cataract retinal pigmentary dystrophy Clinical features from OMIM: 191482 Human phenotypes related to Uncombable Hair, Retinal Pigmentary Dystrophy, Dental Anomalies, and [malacards.org]

[…] the 11 symptoms listed below: Short finger Reduced body hair Mental retardation Woolly hair Metacarpal anomaly Dental anomaly Missing teeth Retinal pigmentary dystrophy Juvenile [checkorphan.org]

Uncombable Hair Syndrome

Several conditions are associated with uncombable hair, such as ectodermal dysplasia, retinal dysplasia/pigmentary dystrophy, juvenile cataract, digit abnormalities, tooth [utexas.influuent.utsystem.edu]

Several conditions are associated with uncombable hair, such as ectodermal dysplasia, retinal dysplasia/ pigmentary dystrophy, juvenile cataract, digit abnormalities, tooth [oadoi.org]

Neurofibromatosis Type 2

cataracts OR unilateral vestibular schwannoma PLUS any two of the following: Meningioma Glioma Neurofibroma Schwannoma Juvenile cataracts OR multiple meningiomas (two or [ctf.org]

NF2 PLUS One vestibular schwannoma in a person less than 30 years of age, OR Any two of the following: meningioma, glioma, schwannoma, juvenile cataracts Common symptoms [nfcenter.wustl.edu]

cataract. [ncbi.nlm.nih.gov]

Autosomal Recessive Congenital Cataract 5

And Intellectual Disability, Marinesco-Sjogren Syndrome AR 92 10 of 10 LEMD2 Cataract, Congenital Or Juvenile Cataract AR 93.48 3 of 3 LIM2 Cataract, Multiple Types AR 100 [igenomix.es]

Pande A, Pande J, Asherie N et al. (2000) Molecular basis of a progressive juvenile‐onset hereditary cataract. [els.net]

but also juvenile-onset cataracts. [medsci.org]

RAPADILINO Syndrome

A disease characterized by dermatological features such as atrophy, pigmentation, and telangiectasia and frequently accompanied by juvenile cataract, saddle nose, congenital [abcam.com]

Auguste Rothmund, a German ophthalmologist who described the characteristic rash and juvenile cataracts in his patients. In 1921, Dr. [rarediseases.org]

cataracts Saddle nose Congenital bone defects, including short stature and radial ray anomalies such as absent thumbs Hair growth problems (absent eyelashes, eyebrows and [ipfs.io]

Hereditary Mucoepithelial Dysplasia

HMD should be considered in the differential diagnosis of childhood alopecia, follicular hyperkeratosis, keratoconjunctivitis, juvenile cataracts, gingival hyperemia, restrictive [ncbi.nlm.nih.gov]

HMD should be considered in the differential diagnosis of childhood keratoconjunctivitis, and/or juvenile cataracts associated to multi–epithelial lesions. [iovs.arvojournals.org]

Microcornea

Cataract Juvenile with micro cornea and glucosuria is a rare cataract disorder distinguished by the association of juvenile cataracts, small corneas and excessive glucose [sehat.com]

GLAUCOMA AND ABSENT FRONTAL SINUS SYNDROME CHOOSE Q15.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 722457005 | Juvenile cataract, microcornea, [bioportal.bioontology.org]

juvenile, with microcornea and glucosuria phenotype from the curated OMIM Gene-Disease Associations dataset. [amp.pharm.mssm.edu]

Autosomal Dominant Optic Atrophy and Cataract

Nonnuclear Polymorphic Congenital, Autosomal Dominant DOA - Dominant Optic Atrophy ADCC - Autosomal Dominant Congenital Cataract DJOA - Dominant Juvenile Optic Atrophy ADC [acronymsandslang.com]

cataract-microcornea-renal glucosuria syndrome Juvenile glaucoma Kandori fleck retina Kein Name gefunden Kein Name gefunden Keratoconus Kinetic eyelid anomaly Knobloch syndrome [se-atlas.de]

Recent studies center on juvenile onset cataracts and subsequent sudden death in a religious isolate in North America, on a rare but distinctive form of dominant macular dystrophy [bcm.edu]