EXOTIC LEGENDS HEROIC SUNDARI

BROWN / BLACK ROSETTE - Daughter of Exotic Legends King Titan & Exotic Legends Astarte Grace (Rene). Sundari is still young but WOW look at the glistening GOLD glitter in her coat.

Pedigree includes RW SGC, CH, DCG, RW QGC and more.  She is super soft and super friendly. She has oval, almost round large eyes. She is VERY vocal and talks all the time. SUPER SOFT. She has a full and broad muzzle, and prominent whisker pads. She has a FAT tail, but most importantly she is very seet, loving and gentle. A wonderful example of the breed.

The following are Sundari's Parents results from the testing we have conducted - You can also check out our Sire and Dam page for her parents and her grandparents results. Sundari is 100% clear:

HCM -CLEAR - TITAN 7-5-2019 HCM SCAN.pd

RENE HCM (1).pdf

The following are Sundari 's results from the testing we have conducted:

Acute Intermittent Porphyria (Variant 1) - Negative

Acute Intermittent Porphyria (Variant 2) - Negative

Acute Intermittent Porphyria (Variant 3) - Negative

Acute Intermittent Porphyria (Variant 4) - Negative

Acute Intermittent Porphyria (Variant 5) - Negative

Autoimmune Lymphoproliferative Syndrome - Negative

Burmese Head Defect (Discovered in Burmese) - Negative

Chediak-Higashi Syndrome (Discovered in Persian cats) - Negative

Congenital Adrenal Hyperplasia - Negative

Congenital Erythropoietic Porphyria - Negative 

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

Cystinuria Type 1A - Negative

Cystinuria Type B (Variant 1) - Negative

Cystinuria Type B (Variant 2) - Negative

Cystinuria Type B (Variant 3) - Negative

Dihydropyrimidinase Deficiency - Negative

Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold) - Negative

Factor XII Deficiency (Variant 1) - Negative

Factor XII Deficiency (Variant 2) - Negative

Familial Episodic Hypokalaemic Polymyopathy (Discovered in Burmese) - Negative

GM1 Gangliosidosis - Negative

GM2 Gangliosidosis - Negative

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

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

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

Glutaric Aciduria Type II - Negative

Glycogen Storage Disease (Discovered in Norwegian Forest Cat) - Negative

Hemophilia B (Variant 1) - Negative

Hemophilia B (Variant 2) - Negative

Hyperoxaluria type II - Negative

Hypertrophic Cardiomyopathy (A31P; Discovered in Maine Coon) - Negative

Hypertrophic Cardiomyopathy (Discovered in Ragdoll) - Negative

Hypotrichosis (Discovered in Birman cats) - Negative 

Lipoprotein Lipase Deficiency - Negative

Medication Sensitivity (MDR1) - Negative

Mucopolysaccharidosis Type I - Negative

Mucopolysaccharidosis Type VI (mild form) - Negative

Mucopolysaccharidosis Type VI (severe) - Negative

Mucopolysaccharidosis Type VII - Negative

Mucopolysaccharidosis VII - Negative

Myotonia Congenita - Negative

Polycystic Kidney Disease (PKD) - Negative

Progressive Retinal Atrophy (Discovered in Bengal cats) - Negative

Progressive Retinal Atrophy (Discovered in Persian cats) - Negative

Progressive Retinal Atrophy (rdAc-PRA) - Negative

Pyruvate Kinase Deficiency - Negative

Sphingomyelinosis (Variant 1) - Negative 

Sphingomyelinosis (Variant 2) - Negative

Spinal Muscular Atrophy (Discovered in Maine Coon) - Negative

Vitamin D-Dependent Rickets - Negative

F.I.V. - Negative  

FeLV - Negative 

DNA Coat Color: - 

1. B/B
2. C/C
3. A/A 
4. N/N
5. D/D
6. E/E
7. GLITTER COAT - 2 COPIES