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- Warsaw breakage syndrome | About the Disease | GARD
Warsaw breakage syndrome is a rare genetic condition that affects many parts of the body People with this condition may have trouble growing before and after they are born, and may have a smaller than average head size
- Warsaw breakage syndrome - Wikipedia
Warsaw breakage syndrome Warsaw breakage syndrome (Warsaw syndrome, WABS) is a rare genetic condition Fewer than 10 cases have been reported by 2018 [2] Its clinical manifestations affect several organ systems, and includes microcephaly and severe growth retardation among others
- Warsaw breakage syndrome: MedlinePlus Genetics
Warsaw breakage syndrome is a condition that can cause multiple abnormalities People with Warsaw breakage syndrome have intellectual disability that varies from mild to severe They also have impaired growth from birth leading to short stature and a small head size (microcephaly)
- Warsaw Breakage Syndrome Foundation – Community. Research. Advocacy.
The Warsaw Breakage Syndrome Foundation is a nonprofit organization dedicated to improving the lives of individuals and families affected by Warsaw Breakage Syndrome (WABS) Our foundation aims to empower and support patients by providing resources, advocacy, and community engagement
- Warsaw breakage syndrome - Orphanet
Additional variable features include limb malformations, cardiac anomalies, abnormal skin pigmentation, and recurrent infections, among others The documents contained in this website are presented for information purposes only
- Warsaw Syndrome - GeneReviews® - NCBI Bookshelf
Warsaw syndrome is characterized by the clinical triad of severe congenital microcephaly, growth restriction, and sensorineural hearing loss due to cochlear hypoplasia Intellectual disability is typically in the mild-to-moderate range Severe speech delay is common
- Warsaw Breakage Syndrome: Causes, Symptoms, and Diagnosis
First described based on a patient from Warsaw, the condition is defined by its impact on growth and cellular stability It presents with physical and developmental challenges that appear before birth and continue throughout life, requiring careful diagnosis and management
- Entry - #613398 - WARSAW BREAKAGE SYNDROME; WABS - OMIM
Warsaw breakage syndrome (WABS) is a rare autosomal disorder characterized by severe prenatal and postnatal growth restriction, microcephaly, developmental delay, cochlear anomalies, and sensorineural hearing loss
- Warsaw Breakage Syndrome: Causes, Signs, and Treatment
Warsaw breakage syndrome is a rare genetic disorder that affects a person's overall health It primarily impacts the body's ability to maintain genetic stability and repair damaged DNA This can lead to various health complications and an increased risk of developing cancer
- DDX11-Related Cohesinopathy - GeneReviews® - NCBI Bookshelf
"Warsaw breakage syndrome" refers to the city of origin of the first reported individual and the elevated level of chromosome breakage, similar to Fanconi anemia, reported in some affected individuals [van der Lelij et al 2010]
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