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We have previously described our extensive experiences with clinical genetic and dysmorphology in a plethora of publications. In a previous study, we reported 43 children with uncommon, rare and very rare genetic and hereditary disorders whom were observed during three-year period (2016-2018). In that series , very rare genetic, the case number 104 of Sanjad-Sakati-Richardson-Kirk syndrome in the world, the case number 130 of Townes Brocks syndrome, and the case number 170 of Coffin Siris syndrome in the world. The aim of this paper is to describe our 2019 extraordinary new experiences with genetic disorders and dysmorphic syndromes.…mehr

Produktbeschreibung
We have previously described our extensive experiences with clinical genetic and dysmorphology in a plethora of publications. In a previous study, we reported 43 children with uncommon, rare and very rare genetic and hereditary disorders whom were observed during three-year period (2016-2018). In that series , very rare genetic, the case number 104 of Sanjad-Sakati-Richardson-Kirk syndrome in the world, the case number 130 of Townes Brocks syndrome, and the case number 170 of Coffin Siris syndrome in the world. The aim of this paper is to describe our 2019 extraordinary new experiences with genetic disorders and dysmorphic syndromes.
Autorenporträt
Aamir Jalal Al-Mosawi jest lekarzem-doradc¿ w Krajowym Centrum Szkole¿ i Rozwoju irackiego Ministerstwa Zdrowia i Bagdadzie Medical City. By¿ szefem irackiej siedziby Mi¿dzynarodowego Panelu Naukowców Kopernika (2006-pädziernik 2020). Jest tak¿e cz¿onkiem rady doradczej Mi¿dzynarodowego Stowarzyszenia Szkó¿ Medycznych (IAMC).