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Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.

A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Genetic analysis is crucial for diagnosing ectodermal dysplasia syndromes, and new therapies may help improve skin issues.

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

Habit reversal training effectively treats hair-pulling disorder in both adults and children.

A 4-year-old girl has a rare hair condition causing fragile, short hair.

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

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

Early recognition and multidisciplinary management are crucial for improving outcomes in Parry-Romberg syndrome.

An 8-year-old boy with hair-pulling disorder had a bald patch that was confirmed not to be a fungal infection and was treated with therapy.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Hair shaft disorders often indicate genetic or systemic issues and are managed by minimizing damage.

Trichostasis spinulosa is a rare skin condition with hair-filled plugs in hair follicles.

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

The infant was diagnosed with Rothmund-Thomson syndrome, a rare genetic disorder causing various physical and developmental issues.

Trichorrhexis invaginata can occur with tinea capitis, though it's rare.

Triangular temporal alopecia is a benign hair loss pattern best diagnosed with dermoscopy, with limited treatment options like surgery and hair transplantation.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

Early diagnosis and treatment of nail and skin conditions can improve health and appearance.

Immunocompromised patients can develop skin and hair issues due to a virus.

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

Topical minoxidil can help improve hair in trichonodosis.

A 16-year-old girl with gum overgrowth and excessive hair growth had successful gum surgery and healed well.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

A rare family case of multiple benign hair follicle tumors was identified, highlighting the need to distinguish them from similar conditions.

Trichoepitheliomas can be hard to distinguish from other skin conditions and often start in teenage years.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Trichotillomania is more common in young females and often linked to stress and psychiatric conditions, with hair loss and increased catagen hair observed.