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Saturday - Thursday 07:00 - 19:00
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Dr. Ayman El Hattab

Dr. Ayman El Hattab

QUALIFICATIONS AND WORK EXPERIENCE

Dr. Ayman El-Hattab graduated from Jordan University of Science and Technology, then he continued his postgraduate education in the USA where he obtained three American Boards: the American Board of Pediatrics, the American Board of Clinical Genetics, and the American Board of Medical Biochemical Genetics (Metabolic).

Dr. Ayman El-Hattab is a Fellow of the American Academy of Pediatrics and Fellow of the American College of Medical Genetics. He is also a member of the American Society of Human Genetics, the European Society of Human Genetics, the Society for the Study of Inborn Errors of Metabolism, the Society for Inherited Metabolic Disorders, and the United Mitochondrial Disease Foundation.

Dr. Ayman El-Hattab has more than 10-year experience in the field of genetics and metabolic as he worked in the USA, Saudi Arabia, and the United Arab Emirates.

ACADEMIA AND RESEARCH

Dr. Ayman El-Hattab is also Associate Professor at the College of Medicine in the University of Sharjah. He has over 100 publications in scientific journals. He presented large number of abstracts as posters and oral presentations in several international conferences. He also conducted several clinical trials. His field of research chromosomal abnormalities, inborn errors of metabolism (metabolic diseases), mitochondrial disorders, neurogenetic disorders, cancer genetics, and novel gene-disease discovery.

SERVICES

Dr. Ayman El-Hattab provides clinical care for children with genetic diseases or suspected to have genetic diseases. This care includes clinical evaluation, genetic counseling, and genetic testing.

Genetic evaluation aims to identify the genetic causes of diseases which can help in directing management, providing knowledge about the disease and its prognosis, understanding the inheritance and recurrent risk, and applying prevention.

Among the numerous genetic and inherited conditions that we provide care for are:

  • Developmental delay and intellectual disability.
  • Chromosomal disorders such as Down syndrome and others.
  • Variable genetic and inherited syndromes.
  • Congenital malformations and birth defects.
  • Autism and other behavioral disorders.
  • Metabolic and mitochondrial diseases.
  • Skeletal dysplasias and deformities.
  • Growth failure.
  • Genetic hearing loss.
  • Genetic neurological diseases.
  • Genetic eye diseases.
  • Family history of genetic diseases.