Café-au-lait-Fleck


Fibröse Dysplasie
Tuberöse Sklerose
Neurofibromatose Typ 1
Gorlin-Goltz-Syndrom
Jaffé-Campanacci-Syndrom
Morbus Gaucher
Maffucci-Syndrom
Noonan-Syndrom
McCune-Albright Syndrom
Fanconi-Anämie
Neurofibromatose
Vitamin-B12-Mangel
Bloom syndrome
Russell-Silver syndrome
Chediak-Higashi-Syndrom
congenital naevus
Louis-Bar-Syndrom
Wiskott-Aldrich-Syndrom
Mukopolysaccharidose Typ II
Legius syndrome
Watson syndrome
multiple mucosal neuroma syndrome
Tuberöse Sklerose
Neurofibromatose Typ 1
Gorlin-Goltz-Syndrom
Jaffé-Campanacci-Syndrom
Morbus Gaucher
Maffucci-Syndrom
Noonan-Syndrom
McCune-Albright Syndrom
Fanconi-Anämie
Neurofibromatose
Vitamin-B12-Mangel
Bloom syndrome
Russell-Silver syndrome
Chediak-Higashi-Syndrom
congenital naevus
Louis-Bar-Syndrom
Wiskott-Aldrich-Syndrom
Mukopolysaccharidose Typ II
Legius syndrome
Watson syndrome
multiple mucosal neuroma syndrome
Café au lait spots are a type of pigmented skin lesions which are classically described as being light brown in color.
Conditions associated with them include:
- neurofibromatosis type 1 (NF1)
- Jaffe-Campanacci syndrome
- McCune-Albright syndrome: typically irregular which has been likened to the coast of Maine
- legius syndrome
Siehe auch:
- Fibröse Dysplasie
- Tuberöse Sklerose
- Neurofibromatose Typ 1
- Gorlin-Goltz-Syndrom
- Jaffé-Campanacci-Syndrom
- Morbus Gaucher
- Maffucci-Syndrom
- Noonan-Syndrom
- McCune-Albright Syndrom
- Fanconi-Anämie
- Neurofibromatose
- Vitamin-B12-Mangel
- Bloom syndrome
- Russell-Silver syndrome
- Chediak-Higashi-Syndrom
- congenital naevus
- Louis-Bar-Syndrom
- Wiskott-Aldrich-Syndrom
- Mukopolysaccharidose Typ II
- Legius syndrome
- Watson syndrome
- multiple mucosal neuroma syndrome
