Zentrum für kongenitale Katarakt am Universitätsklinikum Würzburg
Description of facility
Director / Spokesperson
Prof. Dr. J. HillenkampInformation
Care facility for childrenDescription
Das Zentrum für kongenitale Katarakt betreut Patienten ab Diagnosestellung (meist kurz nach Geburt) bis in das jugendliche Alter. Das Team der Universitäts-Augenklinik Würzburg leistet hierbei die Voraussetzungen für operationstechnische Erfahrung, Kontaktlinsenversorgung, Amblyopieprophylaxe und –behandlung, Screening und frühzeitige Erkennung von Komplikationen (Glaukom) sowie die Anbindung an die Frühförderung des Sehens mittels mehrerer optimal ineinander integrierter Teams aus Ärzten, Orthoptistinnen, Optikerinnen und Sekretariat. Die perioperative Betreuung erfolgt in Zusammenarbeit mit der Kinderklinik der Universität Würzburg.
Care provisions
This facility offers the following
- Diagnostic
- Therapy
Contact
Information
0931 20120487
0931 20120494
ak_schielbeh@ukw.de
Website
https://www.ukw.de/behandlungszentren/zentrum-fuer-kongenitale-katarakt/startseite/
Languages
Deutsch
Englisch
Preview of the assigned diseases 4
Abetalipoproteinemia
Juvenile-onset Steinert myotonic dystrophy
Adult-onset Steinert myotonic dystrophy
Oculocerebrorenal syndrome of Lowe
Familial isolated hypoparathyroidism due to impaired PTH secretion
Spastic paraparesis-cataracts-speech delay syndrome
Spastic ataxia-corneal dystrophy syndrome
Retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome
Musculoskeletal disease with cataract
Homocystinuria due to cystathionine beta-synthase deficiency
Gyrate atrophy of choroid and retina
Incontinentia pigmenti
Marinesco-Sjögren syndrome
Marshall syndrome
Meckel syndrome
21q deletion syndrome
Multiple sulfatase deficiency
Neutral lipid storage disease with ichthyosis
Norrie disease
Down syndrome
Turner syndrome
WAGR syndrome
Werner syndrome
Xeroderma pigmentosum
Monosomy X
X-linked Alport syndrome-diffuse leiomyomatosis
Mosaic variegated aneuploidy syndrome
Isolated aniridia
Cataract-intellectual disability-hypogonadism syndrome
Classic galactosemia
Sanfilippo syndrome type A
Sanfilippo syndrome type B
Sanfilippo syndrome type D
Alpha-N-acetylgalactosaminidase deficiency type 3
ALG8-CDG
3-methylglutaconic aciduria type 4
Pseudopseudohypoparathyroidism
Pseudohypoparathyroidism type 1C
DOORS syndrome
Non-distal duplication 10q
Distal duplication 10q
Juvenile cataract-microcornea-renal glucosuria syndrome
Alpha-mannosidosis, adult form
Hallermann-Streiff syndrome
Harrod syndrome
Upper limb defect-eye and ear abnormalities syndrome
Micro syndrome
Microcephaly-microcornea syndrome, Seemanova type
Rhizomelic chondrodysplasia punctata type 1
Rhizomelic chondrodysplasia punctata type 2
Microcephalic primordial dwarfism, Toriello type
Nathalie syndrome
Cyprus facial-neuromusculoskeletal syndrome
Oculodentodigital dysplasia
Oculofaciocardiodental syndrome
Oculocerebral hypopigmentation syndrome, Cross type
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome
De Barsy syndrome
Proteus-like syndrome
Roberts syndrome
Alpha-N-acetylgalactosaminidase deficiency
Cloverleaf skull-multiple congenital anomalies syndrome
Siegler-Brewer-Carey syndrome
Early-onset lamellar cataract
Microcephaly-brachydactyly-kyphoscoliosis syndrome
Cataract-congenital heart disease-neural tube defect syndrome
Oculoskeletodental syndrome
Congenital-onset Steinert myotonic dystrophy
Mevalonic aciduria
Alpha-mannosidosis
Alport syndrome
Aniridia
X-linked intellectual disability, Najm type
Muscle-eye-brain disease
Hallermann-Streiff-like syndrome
Alström syndrome
MRCS syndrome
3-methylglutaconic aciduria type 7
Trisomy 5p
Rhizomelic chondrodysplasia punctata type 5
Familial isolated hypoparathyroidism
Blomstrand lethal chondrodysplasia
Congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome
Hereditary mucoepithelial dysplasia
Leber congenital amaurosis
Apert syndrome
Trichothiodystrophy
Distal duplication 2p
Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
Tricho-retino-dento-digital syndrome
Proximal myotonic myopathy
Cataract-glaucoma syndrome
Coralliform cataract
Infantile spasms-broad thumbs syndrome
Deafness-onychodystrophy syndrome
Oculo-palato-cerebral syndrome
Aymé-Gripp syndrome
Early-onset posterior polar cataract
Ectopia lentis-chorioretinal dystrophy-myopia syndrome
3q26 microduplication syndrome
Erythrocyte galactose epimerase deficiency
Oculocerebral hypopigmentation syndrome, Preus type
Cochleosaccular degeneration-cataract syndrome
Eye defects-arachnodactyly-cardiopathy syndrome
Microcephalic osteodysplastic dysplasia, Saul-Wilson type
Hereditary hyperferritinemia-cataract syndrome
Rhizomelic chondrodysplasia punctata
Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome
Early-onset partial cataract
Early-onset zonular cataract
Total early-onset cataract
Peters plus syndrome
Familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome
Refsum disease
X-linked retinoschisis
Schwartz-Jampel syndrome
Parkes Weber syndrome
Smith-Lemli-Opitz syndrome
Sotos syndrome
Spondylo-ocular syndrome
Developmental malformations-deafness-dystonia syndrome
Familial isolated hypoparathyroidism due to agenesis of parathyroid gland
Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome
Klippel-Trénaunay syndrome
Microphthalmia with brain and digit anomalies
Stickler syndrome
Foveal hypoplasia-presenile cataract syndrome
Distal triplication 15q
Crouzon syndrome
Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome
Alpha-mannosidosis, infantile form
Blau syndrome
Congenital cataract microcornea with corneal opacity
15q overgrowth syndrome
Tetraamelia-multiple malformations syndrome
Osteoporosis-pseudoglioma syndrome
Generalized galactose epimerase deficiency
PYCR1-related De Barsy syndrome
Tetrasomy 5p
Lymphedema-distichiasis syndrome
Absence deformity of leg-cataract syndrome
Trisomy 9p
Angioosteohypertrophic syndrome
Congenital muscular dystrophy, Fukuyama type
X-linked intellectual disability, Armfield type
Cataract-hypertrichosis-intellectual disability syndrome
Cataract-nephropathy-encephalopathy syndrome
Monosomy 13q14
Epidermal nevus syndrome
Severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract
Distal deletion 13q
Monosomy 18p
Aniridia-intellectual disability syndrome
ALDH18A1-related De Barsy syndrome
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome
Monosomy 18q
Wolf-Hirschhorn syndrome
Monosomy 5p
Galactose mutarotase deficiency
Congenital rubella syndrome
2q24 microdeletion syndrome
Congenital cataracts-facial dysmorphism-neuropathy syndrome
Turner syndrome due to structural X chromosome anomalies
Congenital varicella syndrome
Erythrokeratodermia variabilis
Rhizomelic chondrodysplasia punctata type 3
Triploidy
X-linked Alport syndrome
Trisomy 18
Autosomal recessive Stickler syndrome
Deafness-intellectual disability syndrome, Martin-Probst type
Autosomal recessive cerebelloparenchymal disorder type 3
Autosomal recessive Alport syndrome
Autosomal dominant spastic paraplegia type 9A
Fabry disease
Pseudohypoparathyroidism type 1A
Autosomal dominant Alport syndrome
Systemic disease with cataract
Congenital cataract-hearing loss-severe developmental delay syndrome
Rothmund-Thomson syndrome
Rothmund-Thomson syndrome type 1
Early-onset posterior subcapsular cataract
Chromosomal anomaly with cataract
Cerebral disease with cataract
Intellectual disability-cataracts-kyphosis syndrome
Rothmund-Thomson syndrome type 2
Metabolic disease with cataract
Cardiac disease with cataract
Craniolenticulosutural dysplasia
Dentocutaneous disease with cataract
Autosomal dominant deafness-onychodystrophy syndrome
Craniofacial anomaly with cataract
Galactosemia
Stickler syndrome type 1
Neonatal adrenoleukodystrophy
Nance-Horan syndrome
Early-onset sutural cataract
Pulverulent cataract
Cerulean cataract
Early-onset anterior polar cataract
Early-onset nuclear cataract
Cardiomyopathy-cataract-hip spine disease syndrome
Autosomal recessive palmoplantar keratoderma and congenital alopecia
Cataract-ataxia-deafness syndrome
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome
Cataract-aberrant oral frenula-growth delay syndrome
Microspherophakia-metaphyseal dysplasia syndrome
Intellectual disability-cataracts-calcified pinnae-myopathy syndrome
Autoimmune polyendocrinopathy type 1
Fatty acyl-CoA reductase 1 deficiency
Autosomal dominant hypocalcemia
Cerebrotendinous xanthomatosis
Zellweger syndrome
Mosaic monosomy X
Adams-Oliver syndrome
Lathosterolosis
Galactokinase deficiency
Galactose epimerase deficiency
Sanfilippo syndrome type C
CODAS syndrome
COFS syndrome
Vici syndrome
ALG2-CDG
Monosomy 13q34
Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome
Scalp-ear-nipple syndrome
Flynn-Aird syndrome
Mandibuloacral dysplasia
Late-onset Steinert myotonic dystrophy
Childhood-onset Steinert myotonic dystrophy
Hidrotic ectodermal dysplasia
Steinert myotonic dystrophy
Syndromic cataract
Renal disease with cataract
Stickler syndrome type 2
Mucopolysaccharidosis type 3
Relapsing polychondritis
Microcephaly-congenital cataract-psoriasiform dermatitis syndrome
Cataract-microcornea syndrome
Early-onset non-syndromic cataract
Cataract-intellectual disability-anal atresia-urinary defects syndrome
Persistent hyperplastic primary vitreous
Cataract-deafness-hypogonadism syndrome
Hydrocephaly-cerebellar agenesis syndrome
Dahlberg-Borer-Newcomer syndrome
Basel-Vanagaite-Smirin-Yosef syndrome
Multiple epiphyseal dysplasia, Beighton type
X-linked dominant chondrodysplasia punctata
Pseudohypoparathyroidism with Albright hereditary osteodystrophy
Hypergonadotropic hypogonadism-cataract syndrome
Hypomyelination-congenital cataract syndrome
Trisomy 13
Vogt-Koyanagi-Harada disease
9.95625793933868649.804088878763025Zentrum für kongenitale Katarakt am Universitätsklinikum Würzburg
Last updated:
26.04.2023