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First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

The man's diarrhea was caused by a rare disorder called Cronkhite-Canada syndrome, which improved with specific medications.

The document adds two cases of Gomez-Lopez-Hernandez syndrome and suggests including trigeminal anesthesia and scalp alopecia as key diagnostic criteria.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Two sisters had rare, widespread cysts and complete hair loss, suggesting a genetic link.

Steroids, infection management, and nutritional support can significantly improve symptoms of Cronkhite-Canada Syndrome.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Traditional Chinese medicine may help relieve symptoms of Cronkhite-Canada syndrome.

Low-sulfur hair syndrome can cause UVB sensitivity and testicular failure.

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 woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Prednisone treatment helped a woman with Cronkhite-Canada syndrome recover from hair loss and digestive issues.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

Trichothiodystrophy causes unusual hair and developmental issues.

A woman with chronic hepatitis C had a rare skin condition linked to her illness.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

The report suggests that hair loss in Cronkhite-Canada syndrome may be caused by alopecia areata incognita, as shown by a patient's improvement with treatment.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

Improved nutrition quickly healed the patient's skin lesions.

Routine genetic testing is crucial for early diagnosis and better management of Turner’s syndrome with 21-hydroxylase deficiency.

Cri-du-chat syndrome can cause skin and oral lesions affecting nutrition and quality of life.

Hair loss in Cronkhite-Canada syndrome may be caused by autoimmune factors, not just stress or malabsorption.