seckel syndrome - Axtarish в Google
It is characterized by intrauterine growth restriction and postnatal dwarfism with a small head, narrow bird-like face with a beak-like nose, large eyes.
Seckel syndrome Болезнь или медицинское состояние
Синдром Секкеля, или примордиальная микроцефальная карликовость, является крайне редким врожденным наносомным заболеванием. Наследование аутосомно-рецессивное. Википедия (Английский язык)
Seckel syndrome is characterized by a proportionate dwarfism of prenatal onset, a severe microcephaly with a bird-headed like appearance and mental ...
17 нояб. 2021 г. · Seckel syndrome is rare genetic condition with slow growth before birth (intrauterine growth restriction) resulting in low birth weight. Slow ...
Seckel syndrome is a genetic disorder characterized by growth retardation, very small head (microcephaly( with intellectual disability , and unique facial ...
Seckel syndrome is an extremely rare form of primordial autosomal recessive dwarfism, which is characterised by intrauterine growth retardation, dwarfism, ...
Seckel syndrome, first defined by Seckel in 1960, is characterized by microcephaly, proportionate dwarfism of prenatal onset, and a typical “bird-headed” ...
Seckel syndrome is a rare autosomal recessive disorder characterized by intrauterine growth retardation, dwarfism, microcephaly with mental retardation, ...
8 мая 2024 г. · Seckel syndrome is a rare form of dwarfism characterized by small but proportionate size, a distinctively small head, and severe mental ...
Seckel syndrome is a rare autosomal recessive disorder with stunted growth with intrauterine growth retardation, microcephaly with mental retardation, dwarfism, ...
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