









🩺 Geriatrics Clinic Our Geriatrics Clinic, which aims to protect the physical, mental and social health of elderly individuals, offers a holistic evaluation and treatment service to our elderly patients with its experienced physician staff.

❤️ Pediatric Cardiology Clinic We offer safe, comfortable and modern healthcare services to our children with our expert team in the diagnosis and treatment of congenital or acquired heart diseases.

🎗️ Oncology Clinic Our Oncology Clinic, which provides services with state-of-the-art devices and a multidisciplinary approach in cancer diagnosis and treatment, aims to offer our patients a hopeful recovery process.

🩸 Hematology Clinic Specializing in the diagnosis, treatment and follow-up of blood diseases, our Hematology Clinic provides personalized care to its patients in line with scientific and ethical values.
Annual total inspection data
Definition: Ulcerative proctitis is an inflammatory disease of the rectum and is a form of ulcerative colitis that affects only the rectum. Symptoms: Rectal bleeding, increased bowel movements, rectal pain, mucus-stained stools. Causes:
Definition: Möbius syndrome is a congenital syndrome characterized by facial paralysis and limited eye movements. Symptoms: Facial paralysis, Abducens palsy, difficulty swallowing, Extremity anomalies. Causes: Sporadic,
Definition: VATER/VACTERL association is a syndrome characterized by the association of vertebral, anal, cardiac, tracheoesophageal, renal, and limb anomalies. Symptoms: Vertebral anomalies, anal atresia, cardiac defects, and tracheoesophageal fistula.
Definition Turner syndrome is a chromosomal disorder characterized by short stature, ovarian failure, and various somatic anomalies resulting from the complete or partial loss of an X chromosome.
Definition: Diastrophic dysplasia is a rare skeletal dysplasia characterized by short stature, limb deformities, and ear deformities. Symptoms: Short stature, limb deformities, ear deformities, scoliosis, and causes.
Definition Tyrosinemia type I is a metabolic disease characterized by a deficiency of the enzyme fumarylacetoacetase, leading to liver failure and renal tubular dysfunction. Symptoms: Liver failure, Renal Fanconi