22 мая 2023 г. · People with Wolf-Hirschhorn syndrome experience delayed growth and development. Slow growth begins before birth, and affected infants tend to ...

25 июл. 2024 г. · Wolf-Hirschhorn syndrome (WHS) is an extremely rare chromosomal disorder caused by a missing piece (partial deletion or monosomy) of the short ...

Wolf–Hirschhorn syndrome (WHS) is a chromosomal deletion syndrome resulting from a partial deletion on the short arm of chromosome 4 [del(4)(p16.3)].

The major features include a characteristic facial appearance, delayed growth and development, intellectual disability, low muscle tone (hypotonia), and ...

30 сент. 2022 г. · Wolf-Hirschhorn syndrome is a genetic condition that occurs when someone is missing genetic material at the tip of one of their chromosome 4s.

A developmental disorder characterized by typical craniofacial features, prenatal and postnatal growth impairment, intellectual disability, severe delayed ...

19 дек. 2023 г. · Wolf-Hirschhorn syndrome (WHS), also known as deletion 4p syndrome, is a disorder caused by irregularities on the short arm of chromosome 4 ...

24 нояб. 2022 г. · Wolf-Hirschhorn syndrome is a rare genetic condition caused when part of chromosome 4 is deleted during a baby's development.

What is Wolf-Hirschhorn syndrome? Wolf-Hirschhorn Syndrome (WHS) is a rare genetic condition that occurs when a small part of chromosome 4 is missing ...

Abstract. Wolf-Hirschhorn syndrome is a rare condition caused by terminal deletions, of variable size, in the short arm of chromosome 4.