請注意！我們已搬到宜蘭壯圍！
請注意！我們已搬到宜蘭壯圍！
請注意！我們已搬到宜蘭壯圍！
一、讓渡制
1.本貓舍採現貓制。可在已公開讓渡的小貓之中挑選，付貓價一半的訂金我們即會為您保留該貓咪。
2.在小貓滿三個半月時付清尾款，我們即會在經醫生評估後，安排滿四個月大時進行絕育手術。
3. 本貓舍僅讓渡絕育貓，因此貓咪須在貓舍待滿四個月，等待絕育手術後約7-10天，在貓舍修養完全後（約四個半月大）才能回到新家。不接受任何理由提早帶貓回家。
4.最遲應於小貓滿五個月前帶回家，超過五個月未帶回家將依情形加收住宿費。
二、讓渡價
1.小貓讓渡價依不同花色及條件定價：具體價錢視各別貓而定
2.讓渡價包含：
✔️TICA綠單
✔️絕育手術
✔️兩劑無佐劑三合一疫苗
✔️驅蟲
✔️基本健康檢查
✔️晶片
✔️完整社會化教育
✔️貓父母五十項遺傳疾病基因*檢測結果陰性（含PKD、HCM）
✔️定型化契約
✔️一輩子的娘家照應
3.付款方式包含：
🐾現金
🐾國內匯款
🐾國際匯款
🐾中租無卡分期
*遺傳疾病基因檢測項目：
-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
-Chediak-Higashi Syndrome (Discovered in Persian cats)
-Congenital Adrenal Hyperplasia
-Congenital Erythropoietic Porphyria
-Congenital Myasthenic Syndrome
-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)
-Glutaric Aciduria Type II
-Glycogen Storage Disease
-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)
-Hemophilia B (Variant 1)
-Hemophilia B (Variant 2)
-Hyperoxaluria type II
-Hypertrophic Cardiomyopathy (Discovered in Maine Coon)
-Hypertrophic Cardiomyopathy (Discovered in Ragdoll)
-Hypotrichosis (Discovered in Sacred Birman)
-Lipoprotein Lipase Deficiency
-Mucopolysaccharidosis Type I
-Mucopolysaccharidosis Type VI (G1558A variant)
-Mucopolysaccharidosis Type VI (T1427C variant)
-Mucopolysaccharidosis Type VII
-Mucopolysaccharidosis VII
-Multidrug Resistance 1
-Myotonia Congenita
-Polycystic Kidney Disease (PKD)
-Progressive Retinal Atrophy (rdAc-PRA)
-Progressive Retinal Atrophy (Discovered in Bengal cats)
-Progressive Retinal Atrophy (Discovered in Persian cats)
-Pyruvate Kinase Deficiency
-Sphingomyelinosis (Variant 1)
-Sphingomyelinosis (Variant 2)
-Spinal Muscular Atrophy
-Vitamin D-Dependent Rickets
