Searching for Menkes Support information? Find all needed info by using official links provided below.
http://www.menkes.com/contact-us
Menkes is a multi-disciplinary real estate development company of elegant family homes, exclusive condominiums, and highly coveted office, industrial and retail spaces in the Greater Toronto Area.
https://ghr.nlm.nih.gov/condition/menkes-syndrome
Oct 15, 2019 · Menkes syndrome is inherited in an X-linked recessive pattern.The gene associated with this condition is located on the X chromosome, which is one of the two sex chromosomes.In males (who have only one X chromosome), one altered copy of the gene in each cell is sufficient to cause the condition.In females (who have two X chromosomes), a mutation would have to occur in both copies …
https://themenkesfoundation.org/
Serving as a liaison between families, physicians and researchers with the hope of improving quality care to Menkes children. Support Our Cause Your generous donation will fund our Menkes Awareness campaign and Research initiatives!
Menkes is a multi-disciplinary real estate development company of elegant family homes, exclusive condominiums, and highly coveted office, industrial and retail spaces in the Greater Toronto Area.
http://www.kumc.edu/gec/support/menkes.html
Menkes syndrome, National Center for Biotechnology Information, (NCBI) Genes and Disease Webpage, U.S. National Library of Medicine; Menkes Disease, National Institute of Neurological Diseases and Stroke (NINDS) Menkes Disease, Online Mendelian Inheritance of …
https://rarediseases.info.nih.gov/diseases/1521/menkes-disease
Jul 04, 2017 · The major problems in Menkes disease involve the neurologic, gastrointestinal, and connective tissue (including blood vessels) systems. Pneumonia, leading to respiratory failure, is a common cause of death, although some patients with Menkes disease die suddenly in the absence of any apparent acute medical problem.
https://en.wikipedia.org/wiki/Menkes_disease
Menkes disease (MNK), also known as Menkes syndrome, is an X-linked recessive disorder caused by mutations in genes coding for the copper-transport protein ATP7A, leading to copper deficiency. Characteristic findings include kinky hair, growth failure, and nervous system deterioration.Like all X-linked recessive conditions, Menkes disease is more common in males than in females.Specialty: Endocrinology
https://medlineplus.gov/ency/article/001160.htm
Menkes disease is caused by a defect in the ATP7A gene. The defect makes it hard for the body to properly distribute (transport) copper throughout the body. As a result, the brain and other parts of the body do not get enough copper, while it builds up in the small intestine and kidneys.
https://www.cancertherapyadvisor.com/home/decision-support-in-medicine/pediatrics/menkes-syndrome/
Menkes is a lethal, X-linked, multisystemic, progressive disorder of copper metabolism that causes severe epilepsy, developmental delay, hypotonia, failure to thrive, and death in early childhood.Author: Tyler Reimschisel
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