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Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

High doses of cyproterone acetate increase the risk of brain tumors in women, but the risk decreases after stopping the medication.

The document provides a comprehensive index of medical and surgical topics, including hair removal, hair restoration, and various treatments for injuries and conditions.

The document lists plastic surgery events and opportunities from 1997, including awards, workshops, and conferences.

Caspases are enzymes important for both cell death and various non-lethal cell functions, affecting head development and hair growth, with different caspases playing specific roles.

Facial plastic surgery has evolved to focus on less invasive techniques and innovative technologies for cosmetic and reconstructive procedures.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

A baby girl's hair turned straight on one side due to a neck tumor and surgery, but it returned to curly as she recovered.

A woman's chronic headaches and hair loss were cured by treating her syphilis.

The supplement highlighted advancements and challenges in plastic and reconstructive surgery, including the impact of smoking, chemotherapy, and new treatments like Tafluprost for hair loss.

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."

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Some families have a genetic condition where they are born with irregular scalp defects.

Hair follicle transplantation can hide scars but often needs more than one surgery for better results.

Understanding scalp anatomy is crucial for successful and safe scalp surgery.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Some skin diseases and their treatments can negatively affect male fertility.

LAAM caused developmental toxicity in tolerant rats without causing birth defects.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Covers common skin issues in kids, their diagnosis, treatment, and need for specialist care.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.