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Male pomsky

Uchacq et Parentis , France

Price : 800 € - Euro

Ad description:

Little black male carrier of chocolate and possible dilution with fluffy hair is looking for a nice family. He will be mini-sized. Very cuddly and well-balanced.

Features :

  • SIRET : 84156641700025
  • Catégorie d'animauxDogs
  • Breed :Pomsky
  • Reason for publicationFor sale
  • Age of the animalsPuppy (2 to 6 months)
Animal characteristics :

Date of birth : 3/21/24
Gender : male
Microchip number : 250268781221699
Microchip n° of the dam : 250269590921741
Availability : Now
Deposit amount : 160 € - Euro
Terms of payment :

Transfer or cash

Birth type : Born by natural way

No information provided

Adult size : Small (11 - 22 lbs)
Co-habitation with other animals : Yes
Others animals :

Dogs cats

Health test-s (father) : Yes
Test-s conducted (father) :
Cardiac ultrasound
Doppler echocardiography
DNA Identification
Hips dysplasia
Elbows Dysplasia
(PRA) retinal atrophy
(DCM) dilated cardiomyopathy
Shoulder dysplasia
(DVM) degenerative mitral valve disease
Pennhip (dysplasia screening)
(PKD) polycystic kidney disease
(AEP) auditory evoked potentials
(PS) pulmonary stenosis
(CA) cerebellar abiotrophy
(L2HGA) L-2 hydroxyglutaric aciduria
(LAD) lethal acrodermatitis
(BNAT) neonatal ataxia
(SCA) spinocerebellar ataxia
Late onset ataxia (LOA)
(HSF4) hereditary cataract
(NCL) neuronal ceroid-lipofuscinosis
(CYST) cystinuria
(DMS) dermatomyositis
(DM) degenerative myelopathy
Lafora disease
(NDRG1) hereditary polyneuropathy
(CMR) canine multifocal retinopathy
DNA parentage
DNA profile
(HCM) hypertrophic cardiomyopathy
Gangliosidosis
(NPC) niemann-pick C disease
(SMA) spinal muscular atrophy
(GLD) Krabbe disease
(MC) congenital myotonia
Factor XII or XI deficiency
Mucopolysaccharidoses (all types)
(IDIV) intervertebral disc disease
(HUU) hyperuricosuria
(DVL2) Robinow-like syndrome
Health test-s (mother) : Yes
Test(s) performed (mother) :
Cardiac ultrasound
Doppler echocardiography
DNA Identification
Hips dysplasia
Elbows Dysplasia
(PRA) retinal atrophy
(DCM) dilated cardiomyopathy
Shoulder dysplasia
(DVM) degenerative mitral valve disease
Pennhip (dysplasia screening)
(PKD) polycystic kidney disease
(AEP) auditory evoked potentials
(PS) pulmonary stenosis
(CA) cerebellar abiotrophy
(L2HGA) L-2 hydroxyglutaric aciduria
(LAD) lethal acrodermatitis
(BNAT) neonatal ataxia
(SCA) spinocerebellar ataxia
Late onset ataxia (LOA)
(HSF4) hereditary cataract
(NCL) neuronal ceroid-lipofuscinosis
(CYST) cystinuria
(DMS) dermatomyositis
(DM) degenerative myelopathy
Lafora disease
(NDRG1) hereditary polyneuropathy
(CMR) canine multifocal retinopathy
DNA parentage
DNA profile
(HCM) hypertrophic cardiomyopathy
Gangliosidosis
(NPC) niemann-pick C disease
(SMA) spinal muscular atrophy
(GLD) Krabbe disease
(MC) congenital myotonia
Factor XII or XI deficiency
Mucopolysaccharidoses (all types)
(IDIV) intervertebral disc disease
(HUU) hyperuricosuria
(DVL2) Robinow-like syndrome

No information provided

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