Zentrum für seltene angeborene Herzerkrankungen am Deutschen Herzzentrum der Technischen Universität München
Description of facility
Director / Spokesperson
PD Dr. med. C. WolfInformation
Care facility for adults and childrenDescription
Das Deutsche Herzzentrum München ist ein Fachkrankenhaus für Herz- und Kreislauferkrankungen.
Träger ist das Bayerische Staatsministerium für Wissenschaft und Kunst, dem das DHM direkt unterstellt ist.
Auftrag des DHM ist die Versorgung herzkranker Kinder, Jugendlicher und Erwachsener. Das DHM betreibt Diagnostik und Therapie nach dem jeweils neuesten Stand medizinischer Erkenntnis und trägt durch praxisnahe eigene Forschung zur Weiterentwicklung von Diagnostik- und Therapiekonzepten bei.
Der Leitgedanke des Hauses ist, die verschiedenen zur Diagnostik und Therapie der Herz- und Kreislauferkrankungen erforderlichen Fachrichtungen unter einem Dach zusammenzuführen, damit in ständiger enger interdisziplinärer Zusammenarbeit die Patienten optimal versorgt werden.
Das Zentrum bietet eine multidisziplinäre, evidenz-basierte Diagnostik sowie Beratung und klinische Versorgung von Kindern, Jugendlichen und Erwachsenen mit seltenen angeborenen Herzerkrankungen.
Träger ist das Bayerische Staatsministerium für Wissenschaft und Kunst, dem das DHM direkt unterstellt ist.
Auftrag des DHM ist die Versorgung herzkranker Kinder, Jugendlicher und Erwachsener. Das DHM betreibt Diagnostik und Therapie nach dem jeweils neuesten Stand medizinischer Erkenntnis und trägt durch praxisnahe eigene Forschung zur Weiterentwicklung von Diagnostik- und Therapiekonzepten bei.
Der Leitgedanke des Hauses ist, die verschiedenen zur Diagnostik und Therapie der Herz- und Kreislauferkrankungen erforderlichen Fachrichtungen unter einem Dach zusammenzuführen, damit in ständiger enger interdisziplinärer Zusammenarbeit die Patienten optimal versorgt werden.
Das Zentrum bietet eine multidisziplinäre, evidenz-basierte Diagnostik sowie Beratung und klinische Versorgung von Kindern, Jugendlichen und Erwachsenen mit seltenen angeborenen Herzerkrankungen.
Consultation hours
nach Vereinbarung.
Care provisions
This facility offers the following
-
Participation in registries
- Genetic counselling
-
Clinical studies / research
- Diagnostic
- Therapy
-
Contact person for patients with an unclear diagnosis
Contact
PD Dr. med. C. Wolf
089 12183005
wolf@dhm.mhn.de
Website
https://www.deutsches-herzzentrum-muenchen.de/klinik-fuer-angeborene-herzfehler-und-kinderkardiologie/zentrum-fuer-seltene-angeborene-herzerkrankungen/
Languages
Deutsch
Englisch
Französisch
Spanisch
Preview of the assigned diseases 7
Hurler syndrome
Fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy
Marfan syndrome type 2
Eosinophilic granulomatosis with polyangiitis
Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
Syndrome associated with hypertrophic cardiomyopathy
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
Hurler-Scheie syndrome
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form
Fabry disease
Primary systemic amyloidosis
Non-familial hypertrophic cardiomyopathy
Combined oxidative phosphorylation defect type 23
Isobutyryl-CoA dehydrogenase deficiency
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form
Dilated cardiomyopathy
Beckwith-Wiedemann syndrome due to 11p15 microduplication
Histiocytoid cardiomyopathy
Congenital disorder of glycosylation with dilated cardiomyopathy
Multiple acyl-CoA dehydrogenase deficiency
Fukutin-related limb-girdle muscular dystrophy R13
Microcephaly-cardiomyopathy syndrome
Hypertrophic cardiomyopathy due to intensive athletic training
Primary localized amyloidosis
AL amyloidosis
Long chain acyl-CoA dehydrogenase deficiency
Very long chain acyl-CoA dehydrogenase deficiency
Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3
Familial dilated cardiomyopathy
Mitochondrial trifunctional protein deficiency
Acyl-CoA dehydrogenase 9 deficiency
Alström syndrome
Hypoplastic left heart syndrome
Neuromuscular disease with dilated cardiomyopathy
Beckwith-Wiedemann syndrome due to NSD1 mutation
Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy
Kearns-Sayre syndrome
Costello syndrome
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15
Mitochondrial disease with dilated cardiomyopathy
HEC syndrome
Dilated cardiomyopathy with ataxia
Glycogen storage disease due to acid maltase deficiency, late-onset
LIMS2-related myopathy
Syndrome associated with dilated cardiomyopathy
Fucosidosis
Beckwith-Wiedemann syndrome due to CDKN1C mutation
Heart-hand syndrome, Slovenian type
Beckwith-Wiedemann syndrome due to 11p15 microdeletion
Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type
Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5
Sensorineural deafness with dilated cardiomyopathy
Glycogen storage disease due to LAMP-2 deficiency
Polyglucosan body myopathy type 1
Jervell and Lange-Nielsen syndrome
Delta-sarcoglycan-related limb-girdle muscular dystrophy R6
Non-familial dilated cardiomyopathy
Cirrhotic cardiomyopathy
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion
PGM1-CDG
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Familial long QT syndrome
Early-onset myopathy with fatal cardiomyopathy
Carvajal syndrome
Timothy syndrome
Romano-Ward syndrome
Erythrokeratodermia-cardiomyopathy syndrome
Mucopolysaccharidosis type 2, severe form
Adult polyglucosan body disease
Noonan syndrome with multiple lentigines
Multiple acyl-CoA dehydrogenase deficiency, mild type
Glycogen storage disease due to acid maltase deficiency
Glycogen storage disease due to glycogen debranching enzyme deficiency
Glycogen storage disease due to glycogen branching enzyme deficiency
Friedreich ataxia
Mucopolysaccharidosis type 2, attenuated form
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome
Noonan syndrome
Leber hereditary optic neuropathy
46,XY complete gonadal dysgenesis
1p36 deletion syndrome
Ebstein malformation of the tricuspid valve
Autosomal dominant Emery-Dreifuss muscular dystrophy
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency
Autosomal recessive Emery-Dreifuss muscular dystrophy
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form
Noonan syndrome-like disorder with loose anagen hair
Barth syndrome
Cardiofaciocutaneous syndrome
Endocardial fibroelastosis
McLeod neuroacanthocytosis syndrome
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency
Alpha-B crystallin-related late-onset myopathy
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
Beckwith-Wiedemann syndrome
Cardiomyopathy-cataract-hip spine disease syndrome
X-linked Emery-Dreifuss muscular dystrophy
Beta-mannosidosis
Beta-sarcoglycan-related limb-girdle muscular dystrophy R4
Kidney tubulopathy-dilated cardiomyopathy syndrome
Mitochondrial DNA-related cardiomyopathy and hearing loss
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form
Emery-Dreifuss muscular dystrophy
Duchenne and Becker muscular dystrophy
DPM3-CDG
Autosomal dominant limb-girdle muscular dystrophy type 1B
Vici syndrome
Brugada syndrome
Isolated congenitally uncorrected transposition of the great arteries
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease
Steinert myotonic dystrophy
Congenitally uncorrected transposition of the great arteries with cardiac malformation
Familial thoracic aortic aneurysm and aortic dissection
MELAS
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
MERRF
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome
Glycogen storage disease due to muscle and heart glycogen synthase deficiency
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
Marfan syndrome
Duchenne muscular dystrophy
Catecholaminergic polymorphic ventricular tachycardia
Becker muscular dystrophy
Diabetic embryopathy
Loeys-Dietz syndrome
Peripartum cardiomyopathy
Familial isolated dilated cardiomyopathy
Leber plus disease
DK1-CDG
Cardiomyopathy-hypotonia-lactic acidosis syndrome
Systemic primary carnitine deficiency
Carnitine-acylcarnitine translocase deficiency
Non-familial rare disease with dilated cardiomyopathy
Rare hypertrophic cardiomyopathy
Congenitally uncorrected transposition of the great arteries with coarctation
Desminopathy
Combined oxidative phosphorylation defect type 17
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
Glycogen storage disease with hypertrophic cardiomyopathy
Tetralogy of Fallot
Mucopolysaccharidosis type 2
Lysosomal disease with hypertrophic cardiomyopathy
Marfan syndrome type 1
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
Rare familial disorder with hypertrophic cardiomyopathy
Mitochondrial disease with hypertrophic cardiomyopathy
Glycogen storage disease due to acid maltase deficiency, infantile onset
Congenitally uncorrected transposition of the great arteries
11.55004946398200848.15303425Zentrum für seltene angeborene Herzerkrankungen am Deutschen Herzzentrum der Technischen Universität München
Last updated:
07.09.2023