The 20 Best Williams Syndrome Doctors in Morocco
Find the Top Williams Syndrome Experts and Specialists
Karim Ouldim practices practicing medicine in Fes, Morocco. Mr. Ouldim is rated as an Experienced expert by MediFind in the treatment of Williams Syndrome. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Chromosome 21q Deletion, Tetralogy of Fallot, Deafness Hypogonadism Syndrome, and Lynch Syndrome.
Laila Bouguenouch practices practicing medicine in Fes, Morocco. Ms. Bouguenouch is rated as an Experienced expert by MediFind in the treatment of Williams Syndrome. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Dyggve-Melchior-Clausen Syndrome, Chromosome 21q Deletion, Ovarian Remnant Syndrome, Mosaicism, and Tissue Biopsy.
Mariam Tajir practices practicing medicine in Oujda-angad, Morocco. Ms. Tajir is rated as an Experienced expert by MediFind in the treatment of Williams Syndrome. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses AEC Syndrome, Acromicric Dysplasia, Rubinstein-Taybi Syndrome, and Micrognathia.
Ihssane El Bouchikhi practices practicing medicine in Fes, Morocco. El Bouchikhi is rated as an Experienced expert by MediFind in the treatment of Williams Syndrome. They are also highly rated in 1 other condition, according to our data. Their clinical expertise encompasses Tetralogy of Fallot, Atrial Septal Defect (ASD), Noonan Syndrome, and RASopathies.
Khadija Belhassan practices practicing medicine in Fes, Morocco. Ms. Belhassan is rated as an Experienced expert by MediFind in the treatment of Williams Syndrome. Her clinical expertise encompasses Tetralogy of Fallot, Atrial Septal Defect (ASD), Atrioventricular Septal Defect, and Noonan Syndrome.
Nisrine Aboussair practices practicing medicine in Marrakesh, Morocco. Aboussair is rated as an Experienced expert by MediFind in the treatment of Williams Syndrome. Their clinical expertise encompasses 1p36 Deletion Syndrome, Hepatocerebral Degeneration, Spinocerebellar Ataxia Type 7, and Chromosome 13q Duplication.
Last Updated: 06/30/2026