Moebius syndrome with macular hyperpigmentation, skeletal anomalies, and hypoplasia of pectoralis major muscle in an Egyptian child

by Rabah M. Shawky, Radwa Gamal, Shaimaa Abdelsattar Mohammad
Published 2015-07-01

Challenges in diagnosis and counseling of a family with two recessive neurometabolic disorders

by Heba S. Abd-Elkhalek, Radwa Gamal, Osama K. Zaki, Solaf M. Elsayed
Published 2016-07-01

Kabuki make-up syndrome with genitourinary anomalies, ophthalmologic features and hyperpigmentation in an Egyptian child

by Rabah M. Shawky, Radwa Gamal, Nayera Mostafa
Published 2017-01-01

Cardiomyopathy in Vici syndrome

by Solaf M. Elsayed, Radwa Gamal
Published 2018-01-01

Christ-Siemens-Touraine syndrome with cleft palate, absent nipples, gallstones and mild mental retardation in an Egyptian child

by Rabah M. Shawky, Radwa Gamal
Published 2016-10-01

Bilateral iris, choroid, optic nerve colobomas and retinal detachment in an Egyptian patient with mild Baraitser–Winter syndrome

by Rabah M. Shawky, Heba Salah Abd-Elkhalek Elabd, Radwa Gamal
Published 2014-01-01

Progress in genetics of coronary artery disease

by Radwa Gamal
Published 2018-01-01

Neurofibromatosis type 1 and multiple sclerosis: Genetically related diseases

by Solaf M. Elsayed, Nagia Fahmy, Radwa Gamal, Mohamed Wafik, Dina Zamzam, Mai Fahmy, Mahmoud Suelam
Published 2017-07-01

C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child

by Rabah M. Shawky, Radwa Gamal
Published 2017-01-01

Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II

by Rabah M. Shawky, Radwa Gamal, Shaimaa Abdelsattar Mohammad
Published 2017-10-01

Berardinelli–Seip syndrome type 2 – An Egyptian child

by Rabah M. Shawky, Radwa Gamal, Neveen S Seifeldin
Published 2015-04-01

Meier–Gorlin syndrome: An additional Egyptian patient with gastroesophageal reflux, hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly

by Rabah M. Shawky, Radwa Gamal
Published 2016-10-01

Meier-Gorlin syndrome: Report of an additional patient with congenital heart disease

by Rabah M. Shawky, Heba Salah Abd-Elkhalek Elabd, Radwa Gamal, Shaimaa Abdelsattar Mohammad, Shaimaa Gad
Published 2014-10-01

Baraitser–Winter syndrome: An additional Egyptian patient with skeletal anomalies, bilateral iris and choroid colobomas, retinal hypoplasia and hypoplastic scrotum

by Rabah M. Shawky, Radwa Gamal, Shaimaa Abdelsattar Mohammad
Published 2016-01-01

Removal notice to “An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings” [Egypt J Med Hum Genet 18 (2017) 393–396]

by Solaf M. Elsayed, Radwa Gamal
Published 2018-10-01

Blepharophimosis, ptosis, epicanthus inversus syndrome type 2 with red hair, lymphedema of lower limbs and kidney stones in an Egyptian patient

by Rabah M. Shawky, Radwa Gamal, Neveen S. Seifeldin
Published 2015-10-01

TEMPORARY REMOVAL: An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings

by Solaf M. Elsayed, Radwa Gamal
Published 2017-10-01

Oral–Facial–Digital Syndrome type VI with self mutilations

by Rabah M. Shawky, Heba Salah Abd-Elkhalek Elabd, Shaimaa Gad, Radwa Gamal, Shaimaa Abdelsattar Mohammad
Published 2014-10-01

Cantu syndrome in an Egyptian child

by Rabah M. Shawky, Radwa Gamal
Published 2018-10-01