Congenital alopecia and nail dystrophy associated with severe function T-cell immunodeficiency in two sibs
- Author
- PIGNATA, C1 ; FIORE, M1 ; GUZZETTA, V1 ; CASTALDO, A1 ; SEBASTIO, G1 ; PORTA, F2 ; GUARINO, A1
[1] Department of Pediatrics, Federico II University, Naples, Italy
[2] Department of Pediatrics, University of Brescia, Brescia, Italy - Source
American journal of medical genetics. = Neuropsychiatric genetics. 1996, Vol 65, Num 2, pp 167-170 ; ref : 24 ref
- Publisher
- Wiley-Liss, New York, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Alopécie Association Dystrophie Etude cas Etude familiale Exploration immunologique Fratrie Immunodéficit Lymphocyte T Nourrisson Ongle Poil Trouble fonctionnel Homme Immunopathologie Maladie héréditaire Peau pathologie
- Keyword (en)
- Alopecia Association Dystrophy Case study Family study Immunological investigation Sibling Immune deficiency T-Lymphocyte Infant Nail(anatomy) Hair Dysfunction Human Immunopathology Genetic disease Skin disease
- Keyword (es)
- Alopecia Asociación Distrofia Estudio caso Estudio familiar Análisis inmunológico Hermandad Inmunodeficiencia Linfocito T Lactante Uña Pelo Trastorno funcional Hombre Inmunopatología Enfermedad hereditaria Piel patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B06 Immunopathology / 002B06D Immunodeficiencies. Immunoglobulinopathies / 002B06D01 Immunodeficiencies
- Discipline
- Immunopathology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 2474337
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
10.1002/(SICI)1096-8628(19961016)65:2<167::AID-AJMG17>3.0.CO;2-O 
https://dx.doi.org/10.1002/(SICI)1096-8628(19961016)65:2<167::AID-AJMG17>3.0.CO;2-O
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