ONE of Exotic Legends (Bengal Cats) new babies - WHAT SHOULD WE NAME HER?


Sepia’s have acquired the nickname ‘snow brown Bengals’ but neither are they truly brown- simply that little bit darker.

Instead, their base coats are cream, beige or light tan coloured with markings that are sepia brown or darker.

Sepia Bengal kittens display these marking from birth- hence this is a way of telling them apart from the snow lynx.

A sepia snow Bengal will have green or golden/orang eyes and a light pinkish nose.

Burmese gene  cb/cb

The following are ___________ results from the testing we have conducted:

HCM - 

Bengal PRA -  

Pyruvate Kinase Deficiency (PK) -   

Acute Intermittent Porphyria (Variant 1) - 

Acute Intermittent Porphyria (Variant 2) -

Acute Intermittent Porphyria (Variant 3) -   

Acute Intermittent Porphyria (Variant 4) -   

Acute Intermittent Porphyria (Variant 5) -   

Autoimmune Lymphoproliferative Syndrome -   

Burmese Head Defect (Discovered in Burmese) -   

Chediak-Higashi Syndrome (Discovered in Persian cats) -  

Congenital Adrenal Hyperplasia -

Congenital Erythropoietic Porphyria -

Congenital Myasthenic Syndrome (Discovered in Devon Rex and Sphynx) - 

Cystinuria Type 1A - 

Cystinuria Type B (Variant 1) - 

Cystinuria Type B (Variant 2) -  

Cystinuria Type B (Variant 3) - 

Dihydropyrimidinase Deficiency - 

Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold) - 

Factor XII Deficiency (Variant 1) -   

Factor XII Deficiency (Variant 2) -

Familial Episodic Hypokalaemic Polymyopathy (Discovered in Burmese) - 

GM1 Gangliosidosis - 

GM2 Gangliosidosis - 

GM2 Gangliosidosis, type II (Discovered in Burmese cats) - 

GM2 Gangliosidosis, type II (Discovered in domestic shorthair cats) -

GM2 Gangliosidosis, type II (Discovered in japanese domestic cats) -

Glutaric Aciduria Type II - 

Glycogen Storage Disease (Discovered in Norwegian Forest Cat) - 

Hemophilia B (Variant 1) - 

Hemophilia B (Variant 2) - 

Hyperoxaluria type II -  

Hypertrophic Cardiomyopathy (A31P; Discovered in Maine Coon) -   

Hypertrophic Cardiomyopathy (Discovered in Ragdoll) -

Hypotrichosis (Discovered in Birman cats) -  

Lipoprotein Lipase Deficiency - 

Medication Sensitivity (MDR1) -

Mucopolysaccharidosis Type I - 

Mucopolysaccharidosis Type VI (mild form) -  

Mucopolysaccharidosis Type VI (severe) -

Mucopolysaccharidosis Type VII - 

Mucopolysaccharidosis VII - 

Myotonia Congenita - 

Polycystic Kidney Disease (PKD) - 

Progressive Retinal Atrophy (Discovered in Bengal cats) -

Progressive Retinal Atrophy (Discovered in Persian cats) -

Progressive Retinal Atrophy (rdAc-PRA) - 

Pyruvate Kinase Deficiency -  

Sphingomyelinosis (Variant 1) - 

Sphingomyelinosis (Variant 2) -

Spinal Muscular Atrophy (Discovered in Maine Coon) -   

Vitamin D-Dependent Rickets - 

F.I.V. - 

FeLV - 

DNA Coat Color - 

  1. B/B ?
  2. cb/cb - SEPIA
  3. Apb/a or Apb/A?
  4. N/N  ?
  5. D/D ?
  6. E/E ?