Pigmentary anomalies in the multiple lentigines syndrome : Is it distinct from LEOPARD syndrome ?
- Author
- ARNSMEIER, S. L1 ; PALLER, A. S1
[1] Departments of Pediatrics and Dermatology, Children's Memorial Medical Center, Northwestern University Medical School, Chicago, Illinois, United States - Source
Pediatric dermatology. 1996, Vol 13, Num 2, pp 100-104 ; ref : 22 ref
- CODEN
- PEDRDQ
- ISSN
- 0736-8046
- Scientific domain
- Dermatology; Pediatrics
- Publisher
- Blackwell, Malden, MA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Etude cas Etude familiale Homme Lentiginose Leopard syndrome Multiple Peau pathologie Trouble pigmentation
- Keyword (en)
- Case study Family study Human Lentiginosis Leopard syndrome Multiple Skin disease Pigmentation disorder
- Keyword (es)
- Estudio caso Estudio familiar Hombre Lentiginosis Leopard síndrome Múltiple Piel patología Trastorno pigmentación
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B08 Dermatology / 002B08B Hereditary diseases of the skin. Congenital diseases of the skin. Haemangioma of the skin, of mucosae and of soft tissue
- Discipline
- Dermatology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3054249
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1111/j.1525-1470.1996.tb01413.x 
https://dx.doi.org/10.1111/j.1525-1470.1996.tb01413.x
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