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Early diagnosis and tailored treatment improve outcomes for non-nutritional rickets.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

A woman had a rare reaction to ear piercing that caused earlobe swelling, which was best treated by removing the piercing and not re-piercing.

Regular endoscopic checks are crucial for Cronkhite-Canada syndrome patients to catch potential cancers early.

Rare seminoma found in a 33-year-old woman with atypical genitalia and no Y chromosome.

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

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

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Children with Vitamin D-dependent rickets type II may have severe dental issues that need a team of specialists for proper care.

Keratoacanthoma is a common, usually non-dangerous skin tumor that looks like squamous cell carcinoma but rarely becomes severe.

The boy's symptoms suggest a possible new medical condition.

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.

Early treatment of a rare scalp infection led to full recovery and hair regrowth.

A Chinese boy's scalp infection from a guinea pig was cured with medication.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Combining PRS with TAFR is promising for treating complex fistulas, with most patients achieving long-term healing.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

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

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Many women in Natal, Brazil, have polycystic ovaries according to ultrasound scans.

A gluten-free diet and removing the parathyroid adenoma helped a girl with coeliac disease and high calcium levels start puberty.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

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.

Surgery on a 68-year-old woman with an ovarian tumor led to reduced hirsutism and normal testosterone levels.

Basal cell carcinoma with matrical differentiation is a rare type linked to hair follicles, with .-catenin important for its development.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Clouston syndrome causes issues with teeth, hair, nails, and skin, and has no cure, but recognition has improved.

Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.