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Paternal drug exposure can harm fertility, pregnancy outcomes, and offspring health, with specific drugs linked to various reproductive issues.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Adrenal disorders can cause lasting brain and behavior issues in children.

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

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

The document is a detailed medical reference on skin and genetic disorders.

A rare skin condition usually on the face was found on a man's heel.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Frontalis suspension surgery using autologous fascia lata is effective for treating unilateral congenital ptosis with poor levator function.

Temporal triangular alopecia is a lifelong condition with hairless patches on the side of the head that may be present from birth.

The surgery for severe congenital ptosis in children is safe and effective, with good long-term results.

Latanoprost can cause eyelash drooping as a side effect.

Temporal triangular alopecia in infants is mostly seen in males at birth, with unique features that help with diagnosis.

A child's toe was saved from a rare condition where hair tightly wrapped around it by performing surgery.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

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

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Tacalcitol ointment effectively improves bilateral nevus comedonicus.

A baby's toe was severely damaged by a hair tourniquet, leading to bone and tendon damage, but improved after surgery and treatment.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Triangular temporal alopecia can occur in adults and should be correctly identified to prevent misdiagnosis.

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

Acitretin helped improve hand mobility and skin condition in a patient.

Lash ptosis is more common and severe in people with congenital eyelid droop than in those with acquired eyelid droop or without eyelid droop.

Tinea capitis is a common scalp infection causing hair loss, mostly in young children.

A 23-year-old man has a benign, non-progressive hair loss patch that doesn't respond to treatment but can be cosmetically treated.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.