News

In this insightful video, a woman shares her personal experience living with Marfan Syndrome, a rare condition that has affected her chest and caused unusually long limbs. She talks about how the ...
Innovative genetic testing methods are reshaping reproductive health, offering early detection of genetic conditions and ...
In adults the joint pain and fatigue associated with hypermobility-type EDS can be misdiagnosed as chronic fatigue syndrome ... 1 for one family's story. A genetics referral, along with a complete ...
For patients with disorders such as autism and schizophrenia, mutations in the same gene could require different treatments, according to new research from Yale School of Medicine (YSM).
You can read more about living with Marfan syndrome in Clarissa’s story. In most cases, an individual will see a specialist doctor to do a full health assessment. This might be a genetics doctor, but ...
Delayed lactogenesis II denotes a longer than usual interval between the colostrum phase and copious milk production, but whereby the mother has the ability to achieve full lactation. Failed ...
Outside magazine The idea behind sleepmaxxing — getting sufficient, good quality sleep — isn’t new, says Aruna Rao, assistant professor of neurology at Johns Hopkins Medicine. “People are finally ...
The Silver-Russell syndrome (SRS) is characterised by severe intrauterine ... was performed in 42 subjects and has identified maternal uniparental disomy of chromosome 7 in four. The phenotype was ...
Editor—Reports of patients with terminal de novo deletions of chromosome 15q26 are rare. Excluding cases of ring chromosome 15 formation with different sized deleted chromosomal segments, only seven ...
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