Medical Services

Medical Services

  • Consultations Obstetrics and Gynecology
  • Prenatal diagnosis
  • Consultations and specialist investigations in neurological disorders
  • Medical imaging services (CT, MRI)
  • Cytogenetic and molecular gene tests
  • Maxillo-facial and dento-alveolar surgery

Obstetrics and Gynecology

Double test

Package: Double test + Early Ecomorphology

Triple test

3D ultrasound, 4D

colposcopy

Fetal monitoring + Ultrasound

Obstetrical ultrasound

Gynecological ultrasound

Morphofetal Ultrasound of Trimmer I

Morphofetal Ultrasound of Quarter II

Ovulation monitoring package

Amniotic puncture

Puncture of coral villities

Fetal echocardiography

 

Genetics Laboratory

Cytogenetic tests

G-banded karyotype from peripheral blood
Fetal G-banded karyotype from amniotic fluid
Fetal G-banded karyotype from tissue
Fetal G-banded karyotype from blood obtained by cordocentesis
Fetal G-banded karyotype from chorionic villus biopsy

 

Molecular genetic tests

DNA purification from blood and tissues
Chromosomal microarray
Paternity test
Achondroplasia (FGFR3, G1138A and G1138C)
21-hydroxylase-deficiency screening for the most common 11 mutations of CYP21A1 gene
Hipocondroplazia (FGFR3, N540K)
FSHR (N680S FSH Receptor mutation)
Non-invasive prenatal testing
Wilson disease
CMV qualitative screening from amniotic fluid or blood
Rubella qualitative screening from amniotic fluid or blood
Toxoplasma qualitative screening from amniotic fluid or blood
Varicella zoster qualitative screening from amniotic fluid or blood
Parvovirus qualitative screening from amniotic fluid or blood

Thrombophilia mutations

Factor V Leiden
Factor II-prothrombin G20210A
PAI-1 4G/5G
MTHFR C677T
MTHFR A1298C
Fibrinogen G-455A
Factor XIII Val34Leu

Sensorineural deafness (GJB 35 delG)

Cystic fibrosis (CFTR – ΔF508)

Package

BASIC – Hereditary thrombophilia (Factor V Leiden + Prothrombin G20210A)
BASIC – Hereditary thrombophilia (Factor V Leiden + Prothrombin G20210A + MTHFR C677T + MTHFR A1298C)
EXTENSIVE – Hereditary thrombophilia (Factor V Leiden + Prothrombin G20210A + MTHFR C677T + MTHFR A1298C + Fibrinogen G-455A + Factor XIII Val34Leu)
Sensorineural deafness (GJB 35delG) + Cystic fibrosis (CFTR ΔF508)

Male infertility tests

AZF microdeletions on chromosome Y
Cystic fibrosis – CFTR ΔF508
Cystic fibrosis – Screening for classic CFTR mutations and IVS 5T/7T/9T polymorphism

Package couple infertility

G-banded karyotype from peripheral blood of both partners
AZF microdeletions on chromosome Y
Thrombophilia mutations: Factor V Leiden, Factor II- Prothrombin G20210A, MTHFR C677T, MTHFR A1298C, PAI-1 4G/5G, Factor XIII Val34Leu

Package male infertility

G-banded karyotype from peripheral blood
AZF microdeletions on chromosome Y

Prenatal genetic diagnosis (from amniotic fluid)

Detection of 13, 18, 21, X and Y aneuploidies using QF- PCR
Detection of 13, 18, 21, X and Y aneuploidies using FISH
Achondroplasia (FGFR3, G1138A and G1138C)
Spinal Muscular Atrophy type I-III (SMN1 homozygous deletions)
Beta-thalassemia
Gaucher disease (GBA)
Alpha-1 antitrypsin deficiency (alleles S and Z)
Cystic fibrosis – classic CFTR mutation screening and IVS8 5T/7T/9T polymorphism
Hypochondroplasia (FGFR3 N540K)
Cystic fibrosis (CFTR ΔF508)
Deafness (GJB 35delG)
Non-syndromic deafness (GJB2 and GJB6)
Wilson disease

Package

G-banded karyotype from peripheral blood + Achondroplasia
G-banded karyotype from amniotic fluid + alfa-1 antitrypsin
G-banded karyotype from amniotic fluid + SMN1 homozygous
G-banded karyotype from amniotic fluid + Beta-thalassemia
G-banded karyotype from amniotic fluid + Gaucher disease
G-banded karyotype from amniotic fluid + Wilson disease
G-banded karyotype from amniotic fluid + hypochondroplasia

Imaging

IRM SITE

Cerebral MRI
Pituitary MRI
Cerebral + cervical spine MRI
Cerebral MRI + TOF (Time of Flight)
Head and Neck MRA (Magnetic Resonance Angiography)
Chest MRI
Thoracic aorta MRA (Magnetic Resonance Angiography)
Abdominal MRI
Abdominal +Pelvic MRI
Abdominal aorta +iliac artery MRI
Pelvic MRI
Spine MRI – one region
Spine MRI – two regions
Whole Spine MRI
Lumbar spine + pelvic region MRI
Extremities MRI – unilateral segment (arm, forearm, thigh, leg)
Hand MRI
Hip MRI
Knee MRI
Bilateral Knee MRI
Shoulder MRI
Bilateral Hand MRI
Lumbar spine + sacroiliac joint MRI
Primovist Contrast Enhancement Liver MRI
MRCP
TOF Acquisition
Contrast Enhancement
Primovist Enhancement
Sacroiliac Joint MRI
Neck MRI
Whole Body MRI
Fetal MRI
Second opinion
CD / DVD

Computed Tomography SITE

Routine Head CT
Sinuses CT
Orbits CT
Bilateral Inner Ear CT
Dental CT
Circle of Willis CTA
Head + Circle of Willis CTA (Computed Tomography Angiography)
Carotid CTA (Computed Tomography Angiography)
Head Routine + Carotid CTA (Computed Tomography Angiography)
Head Routine + Carotid + Circle of Willis CTA (Computed Tomography Angiography)
Soft Tissue Neck CT
Larynx CT
Thorax CT
Abdominal CT
Pelvic CT
Abdominal + Pelvic CT
CT Urography (MPh: native + contrast enhancement + late urography)
Pulmonary Arteries CTA (Computed Tomography Angiography)
Thoracic Aorta CTA (Computed Tomography Angiography)
Abdominal Aorta CTA (Computed Tomography Angiography)
Thoracic + Abdominal Aorta CTA (Computed Tomography Angiography)
Thoracic + Abdominal CT
Thoracic + Abdominal + Pelvic CT
CT bazin osos
Extremities Soft Tissues CT
Joints CT
Aorta Run Off CTA (Computed Tomography Angiography)
Spine (one segment) CT
CT Virtual Colonoscopy
CT Contrast Enhancement
Second opinion
CD / DVD

Neurology

Neurological consultation
Electroencephalography adults
Electroencephalography children
Electroneurographic examination (ENG)
Electromyographic examination (EMG)
Electroneuromigrafic examination + consultation
Visual Evoked Potentials
Motor Evoked Potentials
Auditory Evoked Potentials
Somatosensory evoked potentials

The results obtained through consultations and specialist investigations are primarily oriented to the needs of research objectives.