Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis

Eur J Dermatol. 2014 Nov-Dec;24(6):703-4. doi: 10.1684/ejd.2014.2446.

Affiliations

¹ IDI-IRCCS Biochemistry Laboratory.
² Biomedicine and Prevention laboratory, Tor Vergata University of Rome, Italy.
³ Dermatologic Department, S. Andrea Hospital, S. Vercelli, Italy.
⁴ Clinical and Experimental Medicine Department, University of Piemonte Orientale "A. Avogadro", Novara, Italy.
⁵ National Agency for Evaluation of Universities and Research, Rome, Italy.

PMID: 25514680
DOI: 10.1684/ejd.2014.2446

No abstract available

Publication types

Case Reports
Letter
Research Support, Non-U.S. Gov't

MeSH terms

Base Sequence
Dermatitis, Atopic / complications
Dermatitis, Atopic / diagnosis
Female
Filaggrin Proteins
Humans
Infant
Intermediate Filament Proteins / genetics*
Keratin-6 / genetics*
Pachyonychia Congenita / complications
Pachyonychia Congenita / genetics*
Sequence Deletion*

Substances

FLG protein, human
Filaggrin Proteins
Intermediate Filament Proteins
Keratin-6