Kabuki syndrome is a rare, multisystem disorder characterized by multiple abnormalities including distinctive facial features, growth delays, varying degrees of ... |
1 нояб. 2022 г. · It is characterized by distinctive facial features including arched eyebrows ; long eyelashes ; long openings of the eyelids (long palpebral ... |
| синдром Кабуки Болезнь или медицинское состояние |
Синдром Кабуки — редкое врожденное заболевание генетического происхождения. Он поражает несколько частей тела с различными симптомами и тяжестью, хотя наиболее распространенным является характерный внешний вид лица.
Синдром Кабуки встречается... Википедия (Английский язык)
1 сент. 2022 г. · Kabuki syndrome is a rare genetic disease that can affect your child's facial features, musculoskeletal system and many other organs and body ... |
Children with Kabuki syndrome usually have distinctive facial features, mild to moderate mental impairment and growth problems. Kabuki syndrome can also affect ... |
A rare multiple congenital anomalies/neurodevelopmental disorder characterized by five major features: intellectual disability (typically mild to moderate), ... |
Kabuki syndrome is a rare disorder that affects multiple parts of the body. It is present from birth. Specific symptoms and severity can vary. |
Kabuki syndrome is a rare genetic condition characterised by typical facial features, short stature, developmental delay/intellectual disability, ... |
22 июн. 2024 г. · Kabuki syndrome (KS; also known as Kabuki make-up syndrome and Niikawa-Kuroki syndrome) is a rare inherited genetic syndrome first diagnosed in Japan in 1981. |
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