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Two sisters with rickets and hair loss had a genetic issue with vitamin D processing, and only improved when given phosphorus supplements.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Alopecia areata can be triggered by specific immune cells without genetic or environmental factors.

NonClassic Congenital Adrenal Hyperplasia is a less severe form of a genetic disorder affecting adrenal gland function.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

Vitamin D3 analogs can promote hair growth in mice genetically prone to hair loss.

Some men's prostate tissues have low enzyme levels due to genetic changes, possibly affecting treatment for prostate enlargement.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

External factors like certain shampoos, bacterial infections, and parasites might cause hair defects similar to genetic conditions.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Hirsutism is common body hair growth due to genetics and hormones, and while not a disease, it can be distressing; virilisation includes hirsutism with other male traits and needs medical attention.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

Different types of atopic dermatitis were linked to specific genetic and immune changes, suggesting that severe cases might need stronger immune-targeting treatments.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

Personalized treatments for hair loss are becoming more effective by using genetic information.

Androgenetic alopecia is common hair loss caused by genetics and hormones.