Clinical and histological characterization of hair coat and glandular tissue of Chinese crested dogs

Veterinary Dermatology

Volumn 24, Issue 2, 2013, Pages

  Wiener, Dominique J ^a   Gurtner, Corinne ^a   Panakova, Lucia ^b   Mausberg, Theresa Bernadette ^a   Müller, Eliane J ^a   Drögemüller, Cord ^a   Leeb, Tosso ^a   Welle, Monika M ^a  

^a UNIVERSITY OF BERN   (Switzerland)

^b Institute of Internal Medicine   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; ARTICLE; CLASSIFICATION; DENTITION; DOG; FUNCTIONS OF THE SKIN AND ITS APPENDAGES; GENETICS; HAIR; HISTOLOGY; PHYSIOLOGY; SKIN;

ANIMALS; DENTITION; DOGS; HAIR; SKIN; SKIN PHYSIOLOGICAL PHENOMENA;

ANIMALIA; CANIS FAMILIARIS;

EID: 84874761422     PISSN: 09594493     EISSN: 13653164     Source Type: Journal    
DOI: 10.1111/vde.12008     Document Type: Article

References (29)

1. Mecklenburg L. An overview on congenital alopecia in domestic animals. Vet Dermatol 2006; 17: 393-410.
2. Mecklenburg L. Congenital alopecia. In: Mecklenburg L, Linek M, Tobin DJ, eds. Hair Loss Disorders in Domestic Animals. Oxford: Wiley-Blackwell, 2009; 93-113.
3. Robinson R. Chinese crested dog. J Hered 1985; 76: 217-218.
4. Pinheiro M, Freire-Maia N. Ectodermal dysplasias: a clinical classification and a causal review. Am J Med Genet 1994; 53: 153-162.
5. Priolo M, Laganà C. Ectodermal dysplasias: a new clinical-genetic classification. J Med Genet 2001; 38: 579-585.
6. Reed WB, Lopez DA, Landing BH. Clinical spectrum of anhidrotic ectodermal dysplasia. Arch Dermatol 1970; 102: 134-143.
7. Kere J, Srivastava AK, Montonen O et al. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet 1996; 13: 409-416.
8. Schneider P, Street SL, Gaide O et al. Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A. J Biol Chem 2001; 276: 18819-18827.
9. Drögemüller C, Distl O, Leeb T. Partial deletion of the bovine ED1 gene causes anhidrotic ectodermal dysplasia in cattle. Genome Res 2001; 11: 1699-1705.
10. Ferguson BM, Brockdorff N, Formstone E et al. Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain. Hum Mol Genet 1997; 6: 1589-1594.
11. Srivastava AK, Pispa J, Hartung AJ et al. The tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains. Proc Natl Acad Sci USA 1997; 94: 13069-13074.
12. Casal ML, Jezyk PF, Greek JM et al. X-linked ectodermal dysplasia in the dog. J Hered 1997; 88: 513-516.
13. Casal ML, Scheidt JL, Rhodes JL et al. Mutation identification in a canine model of X-linked ectodermal dysplasia. Mamm Genome 2005; 16: 524-531.
14. Beahrs JO, Lillington GA, Rosan RC et al. Anhidrotic ectodermal dysplasia: predisposition to bronchial disease. Ann Intern Med 1971; 74: 92-96.
15. Clarke A, Phillips DI, Brown R et al. Clinical aspects of X-linked hypohidrotic ectodermal dysplasia. Arch Dis Child 1987; 62: 989-996.
16. Baala L, Hadj Rabia S, Zlogotora J et al. Both recessive and autosomal dominant forms of anhidrotic/hypohidrotic ectodermal dysplasia map to chromosome 2q11-q13. Am J Hum Genet 1999; 64: 651-653.
17. Munoz F, Lestringant G, Sybert V et al. Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder. Am J Hum Genet 1997; 61: 94-100.
18. Monreal AW, Ferguson BM, Headon DJ et al. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nat Genet 1999; 22: 366-369.
19. Headon DJ, Overbeek PA. Involvement of a novel Tnf receptor homologue in hair follicle induction. Nat Genet 1999; 22: 370-374.
20. Headon DJ, Emmal SA, Ferguson BM et al. Gene defect in ectodermal dysplasia implicates a death domain adapter in development. Nature 2001; 414: 913-916.
21. Casal ML, Mauldin EA, Ryan S et al. Frequent respiratory tract infections in the canine model of X-linked ectodermal dysplasia are not caused by an immune deficiency. Vet Immunol Immunopathol 2005; 107: 95-104.
22. Moura E, Cirio SM. Clinical and genetic aspects of X-linked ectodermal dysplasia in the dog - a review including three new spontaneous cases. Vet Derm 2004; 15: 269-277.
23. Drögemüller C, Karlsson EK, Hytönen MK et al. A mutation in hairless dogs implicates FOXI3 in ectodermal development. Science 2008; 321: 1462.
24. Ohyama T, Groves AK. Expression of mouse Foxi class genes in early craniofacial development. Dev Dyn 2004; 231: 640-646.
25. Müntener T, Doherr MG, Guscetti F et al. The canine hair cycle - a guide for the assessment of morphological and immunohistological criteria. Vet Dermatol 2011; 22: 383-395.
26. Garcia C, Poletti E. Scalp biopsy specimens: transverse vs vertical sections. Arch Dermatol 2007; 143: 268.
27. Wang X, Tredget EE, Wu Y. Dynamic signals of hair follicle development and regeneration. Stem Cells Dev 2012; 21: 7-18.
28. Paus R, Müller-Röver S, van der Veen C et al. A comprehensive guide for the recognition and classification of distinct stages of hair follicle development. J Invest Dermatol 1999; 113: 523-532.
29. Lewis JR, Reiter AM, Mauldin EA et al. Dental abnormalities associated with X-linked hypohidrotic ectodermal dysplasia in dogs. Orthod Craniofac Res 2010; 13: 40-47.