Servicii medicale Cost (Lei)
Consult embriologie* 180
Consult genetica (amniocenteza)* 125
Consult postnatal* 155
Consult preconceptional* 155
Consult prenatal* 155
Consultatie genetica* 180
Control genetica* 125
Cariotip blastice periferice 1100
Cariotip CVS (Vilozitati coriale) include si QF-PCR (13,18,21,X,Y) +SMA 2900
Cariotip CVS (Vilozitati coriale) include si QF-PCR (13,18,21,X,Y) cu 24 ore timp de raspuns 1450
Cariotip CVS (Vilozitati coriale) include si QF-PCR (13,18,21,X,Y)+35delG 1800
Cariotip CVS (Vilozitati coriale) QF-PCR (13,18,21,X,Y) 2400
Cariotip Lichid amniotic include si QF-PCR (13,18,21,X,Y) 1450
Cariotip Lichid amniotic include si QF-PCR (13,18,21,X,Y) +SMA 2900
Cariotip Lichid amniotic include si QF-PCR (13,18,21,X,Y) cu 24 ore timp de raspuns 1450
Cariotip Lichid amniotic include si QF-PCR (13,18,21,X,Y) cu 24 ore timp de raspuns + AFP 1450
Cariotip Lichid amniotic include si QF-PCR (13,18,21,X,Y) cu 24 ore timp de raspuns + AFP + Fibroza Chistica (?F508) + Surditate Ereditara (35delG) 1800
Cariotip maduva osoasa 1100
Cariotip Molecular (aCGH ) CVS: include si Cariotip clasic 2300
Cariotip Molecular (aCGH ) CVS: include si QF-PCR (13,18,21,X,Y) cu 24 ore timp de raspuns, Cariotip clasic 2400
Cariotip Molecular (aCGH ) Lichid amniotic: include si Cariotip clasic, AFP 2400
Cariotip Molecular (aCGH ) Lichid amniotic: include si QF-PCR (13,18,21,X,Y) cu 24 ore timp de raspuns, Cariotip clasic, AFP 2300
Cariotip Molecular (aCGH ) Sange periferic: include si Cariotip clasic 2400
Cariotip produs de avort 1300
Cariotip produs de avort + Citomegalovirus (CMV) + Toxoplasma gondii 1900
Cariotip sange fetal 1100
Cariotip sange High Resolution 770
Cariotip sange High Resolution + Microdeletii cromozomul Y (AZF) 20 loci + Fibroza chistica gena CFTR cele mai comune 39 mutatii 2800
Cariotip sange High Resolution + Panel trombolilie (Factorul II + Factorul V Leiden + MTHFR 677 si 1298 + PAI 1 + ACE) + Fraxile X (FRAXA) PCR 2600
Celule NK aspirat endometrial 40
Curs puericultura 50
Detectie ADN de CMV/ERB/VSH 1 si 2/VZV (din sange)-pret per virus 460
Detectie ADN de Toxoplasma gondii (din sange) 460
Determinare Rhesus (Rh) din sange matern 725
Determinare sex fetal din sange matern 725
Determinari din secretia uretrala pentru culturi, Chlamidia, Mycoplasma/Ureaplasma 110
Discheratoza congenital DKC1 3600
Disomie uniparentala û test de familie (Sindromul Prader-Willi, Angelman, Beckwith-wiedeman, Silver-Russell) 2000
Displazie acromesomelica, Tip Maroteaux 3600
Displazie distrofica (SLC26A2) 2700
Displazie ectodermala anhidrotica (IKBKG) 2100
Distrofia musculara Duchenne-Becker (DMD/DMB) Analiza linkage 1450
Distrofia musculara Duchenne-Becker (DMD/DMB) Principalele deletii 1100
Distrofie miotonica 2 û DM2 (ZNF9) 2800
Distrofie miotonica û Maladia Steinert (DMPK) 1450
Distrofie musculara Duchenne-MLPA(Cytogenomic) 1000
Echografie endovaginala cu reconstructie volumetrica a cavitatii uterine* 360
Electrocardiograma 30
Extragere fire 35
Factorul II 220
Factorul II + Factorul V Leiden + MTHFR 677 si 1298 715
Factorul V Leiden 210
Factorul XIII 210
Febra mediteraneana familial û Principalele mutatii 1400
Fenilcetonurie (PAH) 3400
Fibroza Chistica (?F508) + Surditate Ereditara (35delG) 300
Fibroza Chistica (?F508) + Surditate Ereditara (35delG) + Atrofie Musculara Spinala (SMA ) 800
Fibroza chistica gena CFTR cele mai comune 39 mutatii 1200
Fibroza chistica gena CFTR mutatia DF508 200
Fibroza chistica toata gena CFTR sequencing 4800
FISH 15q24 deletion syndrome 1000
FISH 17q21 microdeletion 1000
FISH 17q21 microdeletion 1000
FISH 1p36 deletion syndrome 1000
FISH 22q13 / Phelan-Mcdermid 1000
FISH 2p16 microdeletion 1000
FISH 3q29 microdeletion 1000
FISH 9q22.3 microdeletion 1000
FISH cu probe specifice postnatal 1000
FISH cu probe specifice prenatal 1000
FISH MECP2 / Xq28 1000
FISH NF1 microdeletion syndrome 1000
FISH pt gene de fuziune in leucemii 1000
FISH pt gene de fuziune in leucemii 1000
FISH pt non disjunctie 13,18,21,X,Y, sperma 1350
FISH Sindromul Cri du Chat 1000
FISH Sindromul DiGeorge 800
FISH Sindromul Langer-Giedion 1000
FISH Sindromul Miller-Dieker 1000
FISH Sindromul Prader-Willi / Angelman 1000
FISH Sindromul Rubinstein-Taybi 1000
FISH Sindromul Smith-Magenis 1000
FISH Sindromul Sotos 1000
FISH Sindromul WAGR 1000
FISH Sindromul Williams 1000
FISH Sindromul Wolf-Hirschhorn 1000
Fragile X (FRAXA) PCR 1000
Fragile X (FRAXA, FRAXE) MS-MLPA 1000
Fragmentare ADN, sperma(metoda TUNEL) 750
Gangliosidoza (GLB1) 3400
Hemocromatoza ereditatra Tip1 (clasica) û 12 mutatii 1700
Hemocromatoza ereditatra Tip1 (clasica) û 3 mutatii 1400
Hemofilie A (Factorul VIII) 3400
Hemofilie B (Factorul IX) 3400
Hipercheratoza epidermolitica palmoplantara 2200
Hipocondroplazie gena FGFR3 mutatiile C1620A si C1620G 600
Hipocondroplazie gena FGFR3 mutatiile C1620A si C1620G 600
Hipoplazie adrenala congenitala û AHC 2000
Ihtioza lamelara (TGM1) 4900
IRS1 (Insulin Receptor Substrate 1) 1000
Microdeletii cromozomul Y (AZF) 20 loci 900
Montare sterilet Mirena (inclus sterilet) -Florea 700
MTHFR 677 si 1298 (2 mutatii) 390
NeoBona 2200
Neurofibromatoza Tip 1 (NF 1) 2500
Neurofibromatoza Tip 2 (NF 2) 2500
Niemann-Pick, Tip A 3400
Niemann-Pick, Tip B 3400
Osteogeneza Imperfecta û Tip I (COL1A1) 6200
Osteogeneza Imperfecta û Tip III sau IV (COL1A1) 6200
Osteogeneza Imperfecta û Tip III sau IV (COL1A2) 8800
Pachet ATI (preoperator) 250
Pachet Complet include: Factorul II + Factorul V Leiden + MTHFR 677 si 1298 + PAI 1 + ACE 1000
Pachet evaluare uterina(infertilitate) 1500
Pachet infertilitatea 4100
Pachet screening genito-mamar 750
Pachet Standard: Dublu/Triplu Test + Fibroza Chistica (?F508) + Surditate Ereditara (35delG) 500
PAI 1 200
Pansament/toaleta plaga 30
Peniscopia 200
Prader Willi/Angelman metilare 1000
Prelucrare material biologic seminal / Tesut testicular in laborator 200
PrenatalSafe pentru aneupoidiile 13,18,21,XY 4300
Profil imunologic infertilitate(T/B/NK)-analiza sange 380
Punctie mamara cu ac gros 700
Punctie tiroida-consumabile  
Recoltare si determinare HPV polivalent 250
Recoltare si determinare HPV serotipuri oncogene 350
Retinita pigmentoasa (RHO) 2700
Rubella Virus 1200
Scleroza laterana amiotrifica (SOD1) 3400
Scoala mamelor 150
Screening 20 sindroame microdeletii postnatal 850
Screening 20 sindroame microdeletii prenatal 850
Screening microdeletii/microduplicatii subtelomerice ale cromozomilor 1400
Sindromul Apert (FGFR2) 4000
Sindromul Bloom û Principalele mutatii (BLM) 1700
Sindromul Crigler-Najjar (UGT1A1) 5100
Sindromul Crouzon (FGFR2) 400
Sindromul Dandy-Walker ( deletia ZIC1&ZIC4) 2200
Sindromul Dandy-Walker ( deletia ZIC1&ZIC4) 2200
Sindromul Gilbert (UGT1A1) 1400
Sindromul Gilbert (UGT1A1) 1400
Sindromul Lesch-Nyhan (HPRT1) 2200
Sindromul Rett (MECP2) 2500
Sindromul Smith-Lemli-Opitz (DHCR7) 3400
Sindromul Usher (USH2A) 5100
Sindromul Van der Woude (IRF6) 3400
Sindromul Wiskott-Aldrich (WAS) 3400
Spermocultura 90
Spermograma 110
SRY 300
Surditate ereditara gena GJB2 û regiunea codificatoare (Conexina 26-CX26) 1600
Surditate ereditara gena GJB6 û Conexina 30-CX30 2000
Surditate ereditara genele GJB2, GJB3, GJB6 cele mai comune mutatii 1000
Surditate ereditara mutatia 35delG ale genei GJB2 190
Surditate ereditara mutatia W24X ale genei GJB2 190
Tay-Sachs (HEXA) û Principalele mutatii 1900
Test de migrare 70
Test IHC (pana la 6 anticorpi) 540
Test imunohistochimic pachet 5 piese 550
Test Panorama 1 2500
Test Panorama 2 3250
Test postcoital 40
Test Rapid: QF-PCR (13,18,21,X,Y) 500
Testare pentru ejaculare retrograda (include spermograma si detectare spermatozoizi in urina) 50
Thyroid hormone receptor (THR) 2000
Tratamente medicale 10
Triplu test cu interpretare laborator 290
Vaccin Rhophylac (RH) 350