Search results
May 14, 2024 · Waardenburg syndrome is a rare neurocristopathy, with congenital pigmentary disorder secondary to an abnormal distribution of neural crest-derived melanocytes during embryogenesis resulting in patchy areas of depigmentation. It is considered in the investigation of congenital sensorineural deafness.
May 8, 2024 · Symptoms are vital to arriving at the correct diagnosis and excluding diagnoses that may mimic UNE. Mimicking conditions include: C8 radiculopathy. Lower trunk or medial cord brachial plexopathy. Pancoast tumor and true neurogenic thoracic outlet syndrome.
People also ask
What is Waardenburg syndrome?
What are the symptoms of Hunter syndrome?
How do I know if my child has Hunter syndrome?
Apr 29, 2024 · Often, the first symptoms occur around age 13, when people stop growing. People may have hair loss, early graying, loss of bone density or muscle wasting (atrophy). As the disease progresses, people often have vision problems, skin conditions, diabetes or heart problems.
Apr 23, 2024 · These signs and symptoms are real, and they’re part of the natural transition that your body goes through as your periods come to an end. You were expecting hot flashes, right? Not joint pain and dry eyes?
Apr 23, 2024 · Some will experience the signs and symptoms for just a year or two, while others will be in perimenopause for nearly 10 years before reaching menopause. Most often, women will remain in the perimenopause stage for 4 to 8 years.
3 days ago · Symptomatic dialysis access-associated steal syndrome has been reported in up to 6% of AV access patients ref. Prevalence is higher in brachial artery AV access than in radial artery AV. Other risk factors include 1: diabetes. female sex. coronary artery disease. cerebrovascular disease. hypertension. age >60 years. smoking
May 1, 2024 · Hunter syndrome, also called mucopolysaccharidosis type II, is an inherited genetic disorder that occurs almost exclusively in males. It results from a gene mutation that leads to the buildup of...
