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Renal cystadenocarcinoma and nodular dermatofibrosis (RCND) - German Shepherd

Renal / urinary · Dog

Hereditary syndrome of the German Shepherd combining bilateral nodular dermatofibrosis with renal cysts and, frequently, bilateral renal cystadenocarcinoma. It is caused by a missense mutation in the FLCN gene (folliculin; formerly called BHD), the homologue of the gene for human Birt-Hogg-Dubé disease. Affected animals develop skin and renal lesions that may compromise renal function; a lethal effect in homozygosity has been described.
Inheritance patternAutosomal dominant. Heterozygotes develop the disease; a lethal effect in homozygosity has been described (homozygous offspring non-viable or with a more severe and earlier presentation).
Gene / MutationFLCN (folliculin; gene formerly called BHD) c.764A>G p.(H255R) (XM_005619508.3; CanFam3.1 g.42186445A>G). OMIA:001335-9615. Source: Lingaas et al. 2003 (PMID 14532326).
PenetranceHigh penetrance. Heterozygotes develop the disease; homozygotes, when viable, tend to present more severe and earlier forms, although a lethal effect in homozygosity has been described.
Sample type0,5 - 1 ML Sangre EDTA preferiblemente o 2 Hisopos bucales sin medio de raspado intenso
Codeubwn
Turnaround time15 days
PriceOn request
BreedsPastor alemán

Incidence

Specific to the German Shepherd. The population frequency is low, but the disease is emblematic because of its similarity to human Birt-Hogg-Dubé. No reliable carrier figures are published; limited data.

Clinical signs

- Firm, bilateral and symmetrical skin nodules on the face and limbs
- Bilateral renal cysts
- Renal masses (cystadenocarcinoma) that may be bilateral
- Haematuria and abdominal pain in advanced stages
- Deterioration of renal function with polyuria and polydipsia
- Possible dyspnoea if there is pulmonary metastasis

History

The syndrome was described in the German Shepherd as a familial association of dermal fibrosis and renal neoplasia. Molecular characterisation identified the responsible gene as the canine homologue of BHD, placing the disease as the natural counterpart of human Birt-Hogg-Dubé. This finding allowed the development of a carrier genetic test for the breed.

Breeder management

- Test breeding animals before mating
- Do not use affected animals as breeding stock; if the line is maintained, always mate with clear animals
- Do not mate two carriers or affected animals
- Clinical monitoring of carriers: periodic renal and skin ultrasound
- Communicate the status to buyers

Specialist notes

Differential diagnosis with sporadic renal neoplasms, other hereditary skin syndromes and acquired renal cysts. Skin biopsy and abdominal ultrasound are useful in follow-up. The therapeutic approach is surgical and supportive depending on renal extent.

References

1. Jónasdóttir TJ, Mellersh CS, Klungland H, et al. Genetic mapping of a naturally occurring hereditary renal cancer syndrome in dogs. Proc Natl Acad Sci U S A 2000;97(8):4132-7. PMID: 10759551
2. Lingaas F, Comstock KE, Kirkness EF, et al. A mutation in the canine BHD gene is associated with hereditary multifocal renal cystadenocarcinoma and nodular dermatofibrosis in the German Shepherd dog. Hum Mol Genet 2003;12(23):3043-53. PMID: 14532326
3. OMIA:001335-9615 (FLCN). https://omia.org/OMIA001335/9615/

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Price: On request · Turnaround time: 15 days

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