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A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Mutations in hKAP1 genes may cause hereditary hair disorders.

The treatment successfully reopened blood flow in most patients and extended the use of their dialysis access with low risk.

A rabbit gene important for hair development was identified and detailed.

ADF8 and ADF11 help root hairs grow longer at high pH.

BcFLA1 protein is crucial for root hair growth in response to low phosphate in Brassica carinata.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

A new mouse mutation causes skin and hair defects due to a gene change.

ARWH is a rare hair disorder with no cure, but potential treatments include minoxidil and other therapies.

Avacopan may cause unexpected side effects, so early monitoring is important.

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

New compounds with carborane showed anti-androgen effects similar to flutamide.

N-acetyl-GED may help prevent and partially reverse a process that leads to scarring hair loss.

A super thin DIEP flap can effectively reconstruct scalp defects with good skin coverage and contour.

A new gene mutation linked to a skin condition was found in a Spanish family.

Using tissue expanders for scalp reconstruction in patients with extensive Aplasia Cutis Congenita is effective and has minimal complications.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

The authors suggest a method for hair transplantation in fibrosing alopecia pattern distribution to improve treatment outcomes and cover bald areas.

Defective protein folding due to a mutation is key in ANE syndrome.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

ALRN-6924 may prevent hair loss caused by chemotherapy.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

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A new gene mutation causes a rare type of hair loss.

Surgery successfully treated the ferret's adrenal issue, leading to hair regrowth and improved health.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.