Search

everythinglearnresearchcommunity

for

Search:↓

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Women with PCOS may take longer to get pregnant but can have a normal family size, and should manage their overall health to reduce long-term health risks.

HDPCM treatment healed a baby's congenital skin defect caused by varicella infection.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Modified stem cells that overexpress a specific protein can improve hair growth and reduce hair abnormalities in mice.

Down Syndrome patients with Alopecia Areata often have hypothyroidism and specific immune abnormalities.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Alopecia areata is relatively common in children, has a variable course, and shows different responses to treatment; thyroid testing is recommended for those affected.

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

High doses of Lepidium sativum seed extract are toxic and should be used with caution.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Finasteride shows promise for treating hair loss and excessive hair growth, but more research is needed to confirm its effectiveness and safety.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Stopping the pill and giving birth both caused hair loss.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

The document suggests that hair loss after stopping birth control may be similar to post-pregnancy hair loss and could recur with future pregnancies.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.