Verweise von und zu Marfan syndrome
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- Acrochondrohyperplasia
- Angioid streaks
- Aortic isthmus stenosis
- Aortic valve insufficiency
- Arachnodactyly
- Eye diseases, skin changes
- Cowden syndrome
- Cutis laxa, autosomal recessive, type 1c
- Dermatitis-arthritis syndromes
- Dolichostenomelie
- Dystrophia mesodermalis congenita
- Dystrophia mesodermalis congenita, type marfan
- Elastin gene
- Elastosis perforans serpiginosa
- FBN3 gene
- Glycosylation
- Homocystinuria
- Hyperchondroplasia
- Loeys-dietz syndrome
- Marfan achard syndrome
- MEN 3
- Thrombocytopathy
Verweise zu anderen Artikeln
- Arachnodactyly
- Arachnodactyly, congenital contractile
- Ehlers-danlos syndrome
- Elastosis perforans serpiginosa
- Fbn1 gene
- Homocystinuria
- Cataract
- Klinefelter's syndrome
- Loeys-dietz syndrome
- Fingers of the madonna
- Multiple endocrine neoplasias
- Osteogenesis imperfecta
- Striae cutis distensae