What does WHS mean in Human Genome?

This page is about the meanings of the acronym/abbreviation/shorthand WHS in the Medical field in general and in the Human Genome terminology in particular.

Wolf-Hirschhorn Syndrome

Medical » Human Genome

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Definition

What does WHS mean?

Wolf-Hirschhorn Syndrome
A syndrome caused by large deletions of the telomereic end of the short arm of CHROMOSOME 4 (4p) in Wolf-Hirchhorn syndrome critial regions (WHSCRs). Several candidate genes have been identified including WHSC1 and WHSCH2 which appear to be responsible for the core phenotype and in combination with other linked and unlinked genes determine the severity and inclusion of rarer phenotypes. Most cases have a characteristic cranio-facial defect often referred to as "Greek helmet face" - a combined result of MICROCEPHALY, broad forehead, prominent glabella, HYPERTELORISM, high arched eyebrows, short philtrum and micrognathia. In addition there is mental retardation, growth delays, EPILEPSY, and frequently a wide range of midline and skeletal defects, including HYPOSPADIAS; CONGENITAL HEART DEFECTS; CLEFT LIP; CLEFT PALATE; colobomata; CLUBFOOT; clinodactyly; SCOLIOSIS; and KYPHOSIS.

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"WHS." Abbreviations.com. STANDS4 LLC, 2021. Web. 6 Mar. 2021. <https://www.abbreviations.com/term/55451>.

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