Queen Fanny was something like destiny for me. After I took home my first Ragdoll Queen – Candy, I kept watching her sister Cosette. She was available for a long time, so I started to think of offering home also to her. But the timing was not ideal. And finally she found her family. Later, there was Demi, who I liked so much, but when the timing was ok already, she was already reserved.

The selection of Queen Fanny

Soon, there were litter E and F at the breeder and both litters were interested for me. I knew, I didn´t want to miss them, too. There was a beautiful girl in E litter who I started watching. Then, ladies from F litter got their names – Fatima and Fanny. Those names…

Fatima was called my puppy from F litter who I kept at home and made 6 working exams with her till the age of 4 months. Freya, her sister got name Fanny in her new home. So, Fatima and Fanny were my own puppies and now – these two Ragdoll sisters were there with the same names…

As both Ragdoll ladies were beautiful, and I liked them more than the E lady, both with other variety, I finally decided to offer home to both of them. I also wanted to see, what characteristics they will pass to offspring from 3 different varieties with the same King Jami.

Character of Queen Fanny

Queen Fanny loves to play very much, especially chasing balls and prey toys. She loves to kiss people who she loves – this is something really special what I sooner knew only from my kissing dogs. Fanny enjoys cuddling as a typical Ragdoll.

Color

Queen Fanny is blue bicolor (B/B) , dilution (d/d).

Health results of Queen Fanny

Congenital hypothyroidism (CH) – N/N
Cystinuria – N/N
FXII deficiency (1321delC) – N/N
FXII deficiency (1631G>C) – N/N
Hypertrophic Cardiomyopathy (HCM3) Ragdoll – N/N
MDR1 gene variant (MDR) – N/N
Mucopolysaccharidosis type VI (MPS VI) – N/N
Mucopolysaccharidosis type VII (MPS VII) – N/N
Myotonia congenita – N/N
Polydactyly – Hw variant – N/N
Polydactyly – UK1 & UK 2 variant – N/N & N/N
Polycystic kidney disease (PKD) – N/N
Progressive Retinal Atrophy (rdAc-PRA) – N/N
Acrodermatitis enteropathica (AE) – N/N
Alpha-Mannosidosis (AMD) – N/N
Autoimmune lymphoproliferative Syndrome (ALPS) – N/N
Factor XI Deficiency – N/N
Gangliosidosis (GM1) – N/N
GM2-Gangliosidosis – N/N
Gangliosidosis (GM2) – N/N
Glycogen storage disease (GSDIV) – N/N
Head Defect – N/N
Hypertrophic cardiomyopathy (HCM1) Maine Coon – N/N
Hypertrophic cardiomyopathy (HCM4) Sphynx – N/N
Hypokalemia – N/N
Hypotrichosis/Short Life Expectancy – N/N
Congenital myasthenic syndrom (CMS) – N/N
Osteochondrodysplasie – N/N
Primary congenital glaucoma – N/N
Progressive Retinal Atrophy (PRA-b) – N/N
Progressive Retinal Atrophy (pd-PRA) – N/N
Pyruvatkinase Deficiency – N/N
Feline Spinal Muscular Atrophy (SMA) – N/N