Genetic studies of congenital hypotrichosis with anodontia in German Holstein calves;Genetische untersuchung von kongenitaler hypotrichose mit anodontie bei Deutschen Holstein kälbern

Tierarztliche Umschau

Volumn 55, Issue 2, 2000, Pages 72-79

  Von Distl, O ^a   Drogemuller C ^b   Kuiper, H ^b   Kutschke, L ^b   Hermanns, W ^b   Kehler, W ^b   Scholz, H ^b  

^a UNIVERSITY OF VETERINARY MEDICINE HANNOVER   (Germany)

^b NONE

Author keywords

Anodontia; Cattle; Hypotrichosis; Inheritance

Indexed keywords

EID: 0039007930     PISSN: 00493864     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (16)

1. Ansari, H. A., R. Hediger, V. Braun, U. Süss und G. Stranzinger (1987): A case of partial Xq-deletion in a viable hairless calf. Ann. Meet. Amer. Soc. Animal Sci. (Abstr.) 79, 193.
2. Bayes, M., A. J. Hartung, S. Ezer et al. (1998): The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats. Hum. Molec. Genet. 7, 1661-1669.
3. Braun, U., H. A. Ansari, F., Hediger et al. (1988): Hypotrichose und Oligodontie, verbunden mit einer Xq-Deletion, bei einem Kalb der schweizerischen Fleckviehrasse. Tierärztl. Praxis 16, 39-44.
4. Casal, M. L., P. F. Jezyk, J M. Greek et al. (1997): X-linked ectodermal dysplasia in the dog. J. Hered. 88, 513-516.
5. Cole, L. J. (1919): A defect of hair and teeth in cattle - probably hereditary. J. Heredity 10, 303-306.
6. Drieux, H., M. Priouzeau, G. Thiéry und M.-L. Priouzeau (1950): Hypotrichose congénitale avec anodontie, acérie et macroglossie chez le veau. Rec. Méd. Vét. 126, 385-399.
7. Ferguson, B. M., N. Brockdorff, E. Formstone et al. (1997): Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain. Hum. Molec. Genet. 6, 1589-1594.
8. Ferguson, B. M., N. S. T. Thomas, F. Munoz et al. (1998): Scarcity of mutations detected in families with X-linked hypohidrotic ectodermal dysplasia: diagnostic implications. J. Med. Genet. 35, 112-115.
9. Kere J., A. K. Srivastava, O. Montonen et al. (1996): X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nature Genetics 13, 409-416.
10. Monreal, A., B. M. Ferguson, D. J. Headon et al. (1999): Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nature Genetics 22, 366-369.
11. Monreal, A., J. Zonana and B. Ferguson (1998): Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations. Am. J. Hum. Genet. 63, 380-389.
12. Rieck, G. W. (1985): Hypotrichie - Hypodontie - Syndrom beim Rind. Dtsch. Tierärztl. Wschr. 92, 328-329.
13. Solinas-Toldo, S., C. Lengauer und R. Fries (1995): Comparative genome map of human and cattle. Genomics 27, 489-496.
14. Srivastava, A. K., J. Pispa, A. J. Hartung et al. (1997): 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. Nat. Acad. Sci. 94, 13069-13074.
15. Stöber, M., K.-F. Weitze, M. Hoedemaker et al. (1995): Ausgebreitete Minderbehaarung mit horizontalem Vorbiß der Schneidezähne und unterentwickeltem Genitale, eine angeborene Mißbildung beim deutschen Schwarzbunten Rind. Tierärztliche Umschau 50, 224-239.
16. Wijeratne, W. V. S., D. O'Toole, L. Wood and J. W. Harkness (1988): A genetical, pathological and virological study of congenital hypotrichosis and incisor anodontia in cattle. Vet. Record 122, 149-152.