قرار إداري رقم (62) لسنة 2020

   باعتماد أثمان التحاليل المخبرية في مختبرات هيئة الصحة في دبي

ــــــــــــــــــــــــــــــــــــــــــــــــــــــ

 

المدير العام

 

بعد الاطلاع على القانون رقم (14) لسنة 2009 بشأن تسعير الخدمات الحكومية في إمارة دبي وتعديلاته،

وعلى القانون رقم (1) لسنة 2016 بشأن النظام المالي لحكومة دبي،

وعلى القانون رقم (6) لسنة 2018 بشأن هيئة الصحة في دبي، ويُشار إليها فيما بعد بـِ"الهيئة"

وعلى المرسوم رقم (9) لسنة 2012 باعتماد آلية تسعير خدمات هيئة الصحة في دبي،

وعلى المرسوم رقم (17) لسنة 2018 بشأن إنشاء المؤسسات التابعة لهيئة الصحة في دبي وتحديد اختصاصاتها،

وعلى المرسوم رقم (18) لسنة 2018 بتعيين مُدير عام هيئة الصحة في دبي،

وعلى قرار المجلس التنفيذي رقم (18) لسنة 2018 باعتماد الهيكل التنظيمي لهيئة الصحة في دبي،

وعلى القرار الإداري رقم (148) لسنة 2014 بشأن رسوم الخدمات الصحية،

وعلى اعتماد دائرة المالية لأسعار فحوصات مخبرية جديدة المؤرخ في 28/06/2020-مرجع: DOF/OUT/2020/0001504،

 

قررنا ما يلي:

اعتماد الأثمان

المادة (1)

 

تُعتمد بموجب هذا القرار، أثمان التحاليل المخبرية في مختبرات هيئة الصحة في دبي، وفقاً لما هو مبيّن في الجدول المُلحق بهذا القرار.

 

التكليف بالتنفيذ

المادة (2)

 

على كافة الوحدات التنظيمية في الهيئة، اتخاذ الإجراءات اللازمة لوضع هذا القرار موضع التنفيذ، كل في مجال اختصاصه.

 

الإلغاءات

المادة (3)

 

يُلغى أي نص في أي قرار إداري آخر إلى المدى الذي يتعارض فيه وأحكام هذا القرار.

 

السريان والنشر

المادة (4)

 

يُعمل بهذا القرار من تاريخ صدوره، ويُنشر في الجريدة الرسمية.

 

 

 

 

حميد القطامي

المدير العام

 

صدر في دبي بتاريخ 6 يوليو 2020 م

المـــــــــــــــــوافق 15 ذو القعدة 1441 هـ

 

 

 

 

 

 

 

 

 

 

 

 

جدول بتحديد أثمان التحاليل المخبرية في مختبرات هيئة الصحة في دبي

 

S.NO:

Service Code

Service Description

Proposed Price

1

81214

BRCA1 (breast cancer 1) (eg, hereditary breast and ovarian cancer) gene analysis; full sequence analysis and common duplication/deletion variants (ie, exon 13 del 3.835kb, exon 13 dup 6kb, exon 14-20 del 26kb, exon 22 del 510bp, exon 8-9 del 7.1kb)

6490

2

81408

Molecular pathology procedure, Level 9 (eg, analysis of > 50 exons in a single gene by DNA sequence analysis) FBN1 (fibrillin 1) (eg, Marfan syndrome), full gene sequence NF1 (neurofibromin 1) (eg, neurofibromatosis, type 1), full gene sequence RYR1 (ryanodine receptor 1, skeletal) (eg, malignant hyperthermia), full gene sequence VWF (von Willebrand factor) (eg, von Willebrand disease types 1 and 3), full gene sequence

6511

3

81407

Molecular pathology procedure, Level 8 (eg, analysis of 26-50 exons by DNA sequence analysis, mutation scanning or duplication/deletion variants of > 50 exons, sequence analysis of multiple genes on 1 platform) SCN1A (sodium channel, voltage-gated, type 1, alpha subunit) (eg, generalized epilepsy with febrile seizures), full gene sequence

8545

4

2008127

ANTI SACCHAROMYCES CEREVI. ABS

174

5

2090018

Aicardi-Goutières syndrome (NGS)

6830

6

2090019

Aldosterone-Sensitive Distal Nephron (NGS)

6830

7

2090020

Alport syndrome (NGS)

6830

8

2090021

Amyotrophic lateral sclerosis (ALS) (NGS)

10430

9

2090022

Angelman -like syndrome (NGS)

8630

10

2090023

Aortopathy (NGS)

10430

11

2090024

Cardiomyopathy (ARVD/ARVC)/Arrhythmogenic right ventricular dysplasia (NGS)

8630

12

2090025

Ataxia (NGS)

10430

13

2090026

Ataxic polyneuropathies (NGS)

10430

14

2090027

Auditory neuropathy (NGS)

6830

15

2090028

Burkitt lymphoma (NGS)

6830

16

2090029

C3-Glomerulopathies (C3G) (NGS)

8630

17

2090030

Cardiofaciocutaneous syndrome (NGS)

8630

18

2090031

Cardiomyopathy, dilated (NGS)

10430

19

2090032

CFHR5-Nephropathy (NGS)

8630

20

2090033

Chondrodysplasia punctate (NGS)

6830

21

2090034

Congenital disorders of glycosylation (CDG) (NGS)

10430

22

2090035

Congenital heart defects (NGS)

10430

23

2090036

Corneal dystrophies (NGS)

8630

24

2090038

Craniosynostosis syndromes (NGS)

10430

25

2090039

Cutaneous T-cell lymphoma (NGS)

6830

26

2090040

Cystinuria (NGS)

6830

27

2090041

Dent syndrome (NGS)

6830

28

2090042

Diabetes insipidus (NGS)

6830

29

2090043

Diabetes mellitus,monogenic (NGS)

10430

30

2090044

Diffuse large B-cell lymphoma (NGS)

8630

31

2090045

Disorders of sex development (DSD (NGS)

10430

32

2090046

Dyskeratosis congenita (NGS)

8630

33

2090047

Dystonie (NGS)

10430

34

2090048

Ectodermal dysplasia (NGS)

10430

35

2090049

Ellis-van-Crefeld syndrome (NGS)

7280

36

2090050

Epidermolysis bullosa (NGS)

8630

37

2090051

Epilepsy (NGS)

10430

38

2090052

Epilepsy, metabolic (NGS)

10430

39

2090053

Fanconi anemia (NGS)

8630

40

2090054

Fatty acid oxidation disorders (NGS)

8630

41

2090055

Follicular lymphoma (NGS)

6830

42

2090056

Frontotemporal dementia (NGS)

8630

43

2090057

Glucocorticoid Deficiency (NGS)

6830

44

2090058

Familial Gluconeogenesis (NGS)

6830

45

2090059

Glycogen Storage Disease (NGS)

7223

46

2090060

Growth Hormone Deficiency (NGS)

10430

47

2090062

Hereditary sensory and autonomic neuropathy (HSAN) (NGS)

8630

48

2090063

Hermansky-Pudlak syndrome (NGS)

6830

49

2090064

Holoprosencephaly Hyperekplexia (NGS)

6830

50

2090065

Hyperoxaluria Hypertriglyceridemia (NGS)

6830

51

2090066

Familial Hypoglycemia (NGS)

10430

52

2090067

Hypogonadotropic hypogonadism (NGS)

8630

53

2090068

Hypophosphatemic rickets/Phosphate diabetes (NGS)

8630

54

2090069

Ichthyosis and related disorders of cornification (NGS)

10430

55

2090070

Cholestasis, progressive familial intrahepatic (NGS)

6830

56

2090071

Kartagener syndrome (NGS)

10430

57

2090072

Ketogenesis disorder (NGS)

6830

58

2090073

Ketolysis disorder (NGS)

6830

59

2090074

Left ventricular noncompaction (NGS)

6830

60

2090075

Leigh syndrome (NGS)

10430

61

2090076

Acute Myeloid Leukemia (NGS)

8630

62

2090077

Atypical Chronic Myeloid Leukemia (NGS)

6830

63

2090078

Chronic Myelomonocytic Leukemia (NGS)

6830

64

2090079

Chronic Neuthrophilic Leukemia (NGS)

6830

65

2090080

Leukodystrophy (NGS)

10430

66

2090081

T-cell acute lymphoblastic Leukemia (NGS)

8630

67

2090082

Limb-girdle muscular dystrophy (LGMD) (NGS)

10430

68

2090083

Lissencephaly (NGS)

10430

69

2090084

Loeys-Dietz syndrome (NGS)

6830

70

2090085

Lysosomal disorders (NGS)

10430

71

2090086

Macrocephaly (NGS)

10430

72

2090087

Malignant Hyperthermia (NGS)

6830

73

2090088

Mantle Cell Lymphoma (NGS)

6830

74

2090089

Medullary Cystic Kidney Disease (MCKD) (NGS)

6830

75

2090090

Micromelic Dysplasia (NGS)

10430

76

2090091

Metaphyseal dysplasia (NGS)

6830

77

2090092

Mitochondrial encephalopathy (NGS)

10430

78

2090093

Morbus Waldenström (NGS)

6830

79

2090094

mtDNA Depletion/Integrity panel (NGS)

6830

80

2090095

Mucopolysaccharidosis (NGS)

8630

81

2090096

Multiple Epiphyseal Dysplasia and Pseudoachondroplasia (NGS)

6830

82

2090097

Multiple Myeloma (NGS)

6830

83

2090098

Muscular Dystrophies,Congenital (NGS)

10430

84

2090099

Myasthenic Syndrome, Congenital (NGS)

8630

85

2090100

Myelodysplastic syndrome (NGS)

10430

86

2090101

Myopathy, Distal (NGS)

10430

87

2090103

Myotonia (NGS)

6830

88

2090104

Nephrocalcinosis (NGS)

10430

89

2090105

Neurodegeneration with Brain Iron Accumulation (NBIA) (NGS)

8630

90

2090106

Neurofibromatosis (NF) (NGS)

6830

91

2090107

Neuronal Migration Disorder (NGS)

10430

92

2090108

NK/T-Cell Lymphoma (NGS)

6830

93

2090109

Nystagmus (NGS)

6830

94

2090110

Obesity (NGS)

10430

95

2090112

Pancreas Carcinoma (NGS)

8630

96

2090113

Pancreatitis, Chronic (NGS)

6830

97

2090114

Parkinson Disease (NGS)

13966

98

2090115

Pena-Shokeir Syndrome (NGS)

8630

99

2090116

Pendred Syndrome (NGS)

8630

100

2090117

Periodic Fever Syndromes/Autoinflammation (NGS)

10430

101

2090118

Peripheral T-Cell Lymphoma (NGS)

6830

102

2090119

Perrault Syndrome (NGS)

6830

103

2090120

Polymicrogyria (NGS)

8630

104

2090121

Pontocerebellar Hypoplasia (NGS)

6830

105

2090122

Porphyria (NGS)

6830

106

2090123

Progeria Syndromes (NGS)

8630

107

2090124

Progressive External Ophthalmoplegia (PEO) (NGS)

8630

108

2090125

Prostate Cancer (NGS)

10430

109

2090126

Pulmonary Hypertension (NGS)

6830

110

2090127

Pyruvate Dehydrogenase Deficiency (NGS)

6830

111

2090128

Rasopathies (NGS)

8630

112

2090129

Refsum Syndrome (NGS)

8630

113

2090131

Renal Carcinoma (NGS)

8630

114

2090132

Retinitis Pigmentosa (NGS)

10430

115

2090133

Retinoblastoma (NGS)

6830

116

2090134

SANDD Syndrome (NGS)

6830

117

2090135

Schizencephaly (NGS)

6830

118

2090136

Short Stature (NGS)

8630

119

2090137

Skeletal Dyplasia with Abnormal Bone Density/Mineralisation (NGS)

8630

120

2090138

Spastic Paraplegia (NGS)

10430

121

2090139

Spinal Muscular Atrophy, Distal (NGS)

10430

122

2090140

Splenic Marginal Zone Lymphoma (NGS)

6830

123

2090141

Spondylometaphyseal Dysplasia and Spondyloepiphyseal Dysplasia (NGS)

10430

124

2090142

Stargardt Disease (NGS)

6830

125

2090143

Stickler Syndrome (NGS)

6830

126

2090145

Thrombotic Microangiopathy (TMA) (NGS)

8630

127

2090146

Thrombotic Thrombocytopenic Purpura (TTP) (NGS)

8630

128

2090147

Treacher Collins Syndrome (NGS)

6830

129

2090148

Walker-Warburg Syndrome (NGS)

8630

130

2090149

Warburg-Micro Syndrome (NGS)

10430

131

2090150

Xanthinuria (NGS)

6830

132

2090151

Xeroderma Pigmentosum (NGS)

6830

133

2090152

X-linked mental retardation (NGS)

10430

134

2090154

Albinism, Oculocutaneous (MC1R)

1655

135

2090155

Alpha-1-Antitrypsin Deficiency (SERPINA1)

980

136

2090156

Alpha-Thalassemia (HBA, HBA2, sequencing + MLPA)

2780

137

2090157

Pulmonary Alveolar Microlithiasis (SLC34A2)

3680

138

2090158

Amyloidosis, Hereditary, Transthyretin-related (TTR, stage 1)

980

139

2090159

Amyloidosis, Hereditary, Transthyretin-related (TTR, stage 2)

1295

140

2090160

Arthrogryposis (TNNI2)

2105

141

2090161

Arts Syndrome (PRPS1)

2330

142

2090162

Ataxia Teleangiectasia (ATM)

6830

143

2090163

Ataxia Teleangiectasia (ATM, MLPA)

1880

144

2090164

Beta-Propeller Protein-Associated Neurodegeneration (WDR45)

2555

145

2090166

Blepharophimosis (FOXL2)

980

146

2090167

Hypertension and Brachydactyly Syndrome (PDE3A)

5399

147

2090169

Coenzyme Q10 Deficiency (NGS)

8630

148

2090170

Cohesinopathies (e.g. Cornelia de Lange Syndrome) (NGS)

6830

149

2090171

Cowden Syndrome 3 (NGS)

6830

150

2090172

CTNNB1-Associated Diseases (CTNNB1)

3905

151

2090173

Donnai-Barrow Syndrome (LRP2)

6830

152

2090174

Dravet Syndrome (GABRG2)

3455

153

2090176

Ellis-Van-Creveld Syndrome (EVC, EVC2, MLPA)

1880

154

2090177

Encephalopathy Syndrome, Lethal Neonatal Spasticity-Epileptic (BRAT1)

5030

155

2090178

Epileptic Encephalopathy (WWOX)

3005

156

2090180

Fleck Retina, Familial Benign (PLA2G5)

1565

157

2090181

Exudative Vitreoretinopathy (LRP5)

6830

158

2090182

Exudative Vitreoretinopathy Type 1 (FZD4)

1115

159

2090183

Familial Isolated Arrhythmogenic Ventricular Dysplasia (PKP2)

5317

160

2090184

X-Linked Intellectual Disability (OPHN1)

4580

161

2090185

Limb-Girdle Muscular Dystrophy Type 2D (SGCA)

3157

162

2090186

Glioma (POT1) (NGS)

4580

163

2090187

Hemolytic-Uremic Syndrome, Atypical (AHUS3/CFI)

3110

164

2090188

Hemolytic-Uremic Syndrome, Atypical (AHUS5/C3)

5930

165

2090189

Hemolytic-Uremic Syndrome, Atypical (AHUS7/DGKE)

3005

166

2090190

Hermansky-Pudlak syndrome 1 (HPS1)

5030

167

2090191

Hermansky-Pudlak Syndrome 3 (HPS3)

5030

168

2090192

Hermansky Pudlak Syndrome 5 (HPS5)

5030

169

2090193

Hermansky-Pudlak Syndrome 6 (HPS6)

2371

170

2090194

Hermansky-Pudlak Syndrome 8 (HPS8/BLOC1S3)

980

171

2090195

HIV Infection, Susceptibility/Resistance to (CCR5)

980

172

2090196

Corneal Dystrophy (SLC4A11)

5480

173

2090197

Hyper-IgE Syndrome-NGS (NGS)

6830

174

2090198

Hyperlipoproteinemia (APOA5) (NGS)

6830

175

2090199

Hypophosphatemia with Hypercalciuria (SLC34A3)

2555

176

2090200

Hypophosphatemia with Nephrolithiasis or Osteoporosis (SLC34A1)

4008

177

2090201

Hypophosphatemic Rickets, Autosomal Dominant (FGF23, MLPA)

1913

178

2090202

Imerslund-Grasbeck Syndrome (AMN)

3095

179

2090203

Jalili Syndrome (cone-rod retinal dystrophy and amelogenesis imperfecta) (CNNM4)

3026

180

2090204

Jervell- and Lange-Nielsen Syndrome (NGS)

6830

181

2090205

Joubert Syndrome (POC1B)

3905

182

2090206

Campomelic Dysplasia (SOX9, MLPA)

1880

183

2090207

Cataract Syndrome (CRYAA)

1880

184

2090208

Cataract 14, Multiple Types (GJA3)

980

185

2090210

Lathosterolosis (SC5DL)

3680

186

2090211

Legius syndrome (SPRED1)

2465

187

2090213

Lesch-Nyhan syndrome (HPRT1, MLPA)

2371

188

2090215

Lujan-Fryns Syndrome (MED12) (NGS)

6830

189

2090216

Mayer-Rokitansky-Küster-Hauser Syndrome (WNT4)

2015

190

2090217

Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic (PIK3CA )

5930

191

2090218

Microcephaly (ASPM)

6830

192

2090219

Microcephaly (KIF11)

4130

193

2090220

Microcephaly (PCNT)

10430

194

2090221

Microcephaly (RBBP8)

5930

195

2090222

Microcephaly (SLC25A19)

2555

196

2090223

Mitochondrial DNA Depletion Syndrome (DGUOK)

2830

197

2090224

Wilson Disease (ATP7B, Stage 3, MLPA)

1880

198

2090226

Myotonia Congenita Type Becker/Thomsen (CLCN1, MLPA)

2155

199

2090227

Nephronophthisis (NPHP4)

5930

200

2090228

Nephronophthisis-like Nephropathy (NPHPL1/XPNPEP3)

3353

201

2090230

Nephrotic Syndrome (WDR73)

2465

202

2090231

Retinal Dystrophy (RGS9BP)

980

203

2090232

Hereditary Sensory and Autonomic Neuropathy Type 5 (NGF)

1295

204

2090233

Noonan-like Syndrome with Loose Anagen Hair (SHOC2)

3095

205

2090234

Osteopathia Striata, Cranial Sclerosis (AMER1/WTX)

2465

206

2090235

Paralysis, Thyrotoxic Periodic (KCNJ18)

1295

207

2090236

Perrault Syndrome (CLPP)

1880

208

2090237

Perrault Syndrome (LARS2)

4662

209

2090238

Polycystic Liver Disease (GANAB)

6155

210

2090240

Retinol Dystrophy, Iris coloboma, and Comedogenic Acne Syndrome (RBP4)

1655

211

2090241

Retinitis Pigmentosa (IMPG2)

6830

212

2090242

Retinitis Pigmentosa (LRAT)

1115

213

2090243

Retinitis Pigmentosa (NR2E3)

3095

214

2090244

Rett-like syndrome (NTNG1, MLPA)

1880

215

2090245

Rett-like syndrome (NTNG1, Seq.)

2195

216

2090246

Robinow Syndrome (WNT5A)

4355

217

2090247

Deafness (GPSM2)

4580

218

2090248

Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)

6380

219

2090249

Simpson-Golabi-Behmel Syndrome (GPC3) (Testicular Feminization Syndrome)

3353

220

2090251

TARP Syndrome (RBM10)

5930

221

2090254

Hyperphosphatemic Tumoral Calcinosis, Familial (GALNT3)

5534

222

2090255

Vasculopathy, ADA2 Deficiency (CECR1)

3005

223

2090256

Wolman Disease (LIPA)

3005

224

2090257

Cone-Rod Dystrophy (CTNNA1)

4355

225

2090258

Congenital Adrenal Hyperplasia (NGS)

8630

226

2090259

Lysosomal Perioxisomal Disorders NGS

10430

227

2090260

CYP21A2 Deletion & Duplication (MLPA)

1880

228

2090261

Microarray CGH 180 K Amniotic Fluid/CVS

6750

229

2090262

PTEN Gene Amniotic fluid/CVS

2925

230

2090263

Skeletal Dysplasia and Pena Shokeir Syndrome

8630

231

2090264

Methylation Test Russel Siver Syndrome

1880

232

2090265

Ichthyoses and Related Disorder panels

10430

233

2090266

Heteroxy and Situs Inversion Panel

10430

234

2090267

Multi Gene Panel- Mitochondrial

10430

235

2090268

Sister Chromatid Exchange for Bloom Syndrome.

1871

236

2090269

Breast Cancer Mutigene Panel-NGS

8630

237

2090270

Medium Chain Acyl CoA Deficiecy

3905

238

2090271

Gastrointestinal Atresia Panel

6626

239

2090272

KGB Syndrome

3680

240

2090273

Neurofascins Abs.(140 & 155)

1954

241

2090274

Contactin- 1 (CASPR1)

1138

242

2090275

Amlodipine

418

243

2090276

Beta HCG(CSF)

454

244

2090277

Alpha Feto protein (AFP) (CSF)

205

245

2090278

HIV Viral load(CSF)

945

246

2090279

5 Methyl Tetra Hydro folate(CSF)

1221

247

2090280

Pregnanacy Associated Plasma Protein(PAPP-A)

305

248

2090281

Rituximab Neutralizing  Abs

2905

249

2090282

Omega 6 Fatty Acids Screen

306

250

2090283

Chlamydia Trachomatis IgA & IgG  ABS

251

251

2090284

Chlamydia Pneumonia IgM & IgG ABS

251

252

2090285

Zika Virus  IgG/IgM ABS

305

253

2090286

Entero Virus RNA PCR

741

254

2090287

Legionella Culture Specimen

162

255

2090288

Porphyrin

251

256

2090289

Porphobilinogen

251

257

2090290

Pseudomonas Aeruginosa Abs.

445

258

2090291

Oncotype DX (21 GENES)

22080

259

2090292

Iodine Urine

113

260

2090293

Cytomegalovirus PCR CSF

233

261

2090294

Chickengunya Virus RNA PCR

395

262

2090295

Dihydropteridine Reductase (DHPR) Activity

305

263

2090296

Fibroblast Growth Factor 23 Level

180