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Salla Disease

Sandhoff Disease

Sanfilippo Syndrome A

Sanfilippo Syndrome A, B, C and D

Sanfilippo Syndrome B

Sanfilippo Syndrome C

Saposin A Deficiency

Saposin B Deficiency

Saposin C Deficiency

Say-Barber-Biesecker-Young-Simpson syndrome (SBBYSS)

Schopf-Schulz-Passarge Syndrome (SSPS)

Schwannomatosis

Seckel syndrome

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SESAMES/ Enlarged Vestibular Aqueduct (digenic)/ Pendred’s syndrome

Sensorineural Hearing Loss (SNHL)

Septo-Optic Dysplasia

Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans (SADDAN)

Severe Combined Immune Deficiency (SCID)

Severe Combined Immune Deficiency (SCID), ADA Type

Severe Combined Immune Deficiency (SCID), DCLRE1C Type

Severe Combined Immune Deficiency (SCID), IL7R Type

Severe Combined Immune Deficiency (SCID), JAK3 Type

Severe Combined Immune Deficiency (SCID), RAG Type

Severe Combined Immune Deficiency (XSCID), X-linked

Severe Combined Immune Deficiency with Radiation Sensitivity

Severe Congenital Neutropenia

Short QT Syndrome (SQTS)

Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency

Short-Rib Thoracic Dysplasia (SRTD)

Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency

Shprintzen-Goldberg syndrome

Shwachman-Diamond Syndrome (SDS)

Sialidosis

Sideroblastic Anemia

Sideroblastic Anemia with Spinocerebellar Ataxia

Sideroblastic Anemia, X-linked

Simpson-Golabi-Behmel Syndrome (SGBS)

Sinoatrial node dysfunction and deafness (SANDD)/ Bradycardia and congenital deafness/ SNHL

Sjogren Larsson Syndrome (SLS)

Small Fiber Neuropathy (SFN)

Smith-Lemli-Opitz Syndrome

Smith-Magenis Syndrome (SMS)

SNHL (AR)

SNHL and male infertility

Sotos Syndrome

Spastic Ataxia

Spastic Paraplegia 28 (SPG28)

Spastic Paraplegia 4 (SPG4)

Spastic Paraplegia 43 (SPG43)

Spastic Paraplegia 54 (SPG54)

Spastic Paraplegia 74 (SPG74)

Spinal and Bulbar Muscular Atrophy (SBMA)

Spinal Muscular Atrophy with Respiratory Distress Type 1 (SMARD1)

Split Hand - Split Foot Malformation

Spondylometaepiphyseal Dysplasia, Menger Type

Stargardt Disease

Steatocystoma Multiplex

Steinert Disease

Stickler syndrome

Sudden Cardiac Arrest

Sudden Unexplained Death

Superficial Epidermolytic Ichthyosis

Supravalvular Aortic Stenosis

Syndromic Micropthalmia Type 3

HASTALIKLARA GÖRE TESTLER

*Detaylı bilgi için her bir hastalığın üstüne tıklayınız.

*Bizim yapmadığımız testlerin bazılarını çalıştırdığımız, hepsi sertifikalı ve yetkin, tüm yurt dışı ve yurt içi Laboratuvarlar ile anlaÅŸmalıyız. Fiyat indirimi, doku örneklerinin güvenli bir ÅŸekilde eldesi, gönderimi ve takibi, testlerin açıklanması ve hastaya genetik danışmanlığının verilmesi tamamen bize ait sorumluluklardır.

*Hastalıklar zaman zaman orijinal, zaman zaman Türkçe isimleriyle dizinlenmiÅŸtir. Mümkün olduÄŸunca Türkçe açıklamalara yer verilmeye çalışılmıştır. 

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© Copyright 2023 by Dr. Hakan Ulucan "GEN HEKİMİ"

Cumhuriyet Mah Yıldıray Çınar Sok No:21

Büyükçekmece İstanbul

0212 872 13 96

0533 409 25 45

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