Symptoms, Diagnosis, and Treatment for Women and Girls With Hemophilia: A Narrative Review
ABSTRACT Introduction Hemophilia is an X‐linked bleeding disorder previously thought to present only in men. This sentiment is rapidly changing as the information around women and girls’ experiences of bleeding symptoms has evolved, sparking intense discussion among researchers, clinicians, patients, and patient advocates regarding appropriate ...
Sam Hirniak +6 more
wiley +1 more source
Comment on "The Prevalence of Vitamin B12, Hemoglobin, and Ferritin Deficiency in Patients with Morbid Obesity and Changes in their Blood Levels after Bariatric Surgery". [PDF]
Saher L.
europepmc +1 more source
The XX Factor in Hemophilia: Diagnostic, Therapeutic, and Research Gaps for Women and Girls
ABSTRACT Introduction Hemophilia has traditionally been viewed as an X‐linked disorder affecting men and boys, with women and girls labeled as “carriers”, presumed to be clinically unaffected. This paradigm has contributed to under‐recognition, delayed diagnosis, and undertreatment of females with hemophilia‐associated genotypes despite an increasingly
Kelsey Uminski, Ellen Cusano
wiley +1 more source
Micronutrient Networks in Nutritional Anemia: A Narrative Review Beyond Pathophysiology, Diagnosis, and Management of Iron Deficiency. [PDF]
Chougule S +6 more
europepmc +1 more source
Underdiagnosis of Von Willebrand Disease: The Silent Majority of Women in Brazil
Abstract Introduction Von Willebrand disease (VWD) is the most common inherited bleeding disorder. Although autosomal inheritance predicts a similar distribution between sexes, women are more often diagnosed due to hemostatic challenges associated with menstruation and childbirth.
Yara Maria da Silva Pires +2 more
wiley +1 more source
An ironclad case for cost-effective screening in pregnancy. [PDF]
Lewkowitz AK, Auerbach M.
europepmc +1 more source
Racial disparities in anaemia associated with paediatric chronic kidney disease
British Journal of Haematology, EarlyView.
Manya Raina +3 more
wiley +1 more source
Living With Factor VII Deficiency—A Mixed Methods Study
ABSTRACT Background Factor VII deficiency (FVIID) is a rare autosomal recessive disorder, resulting in potentially unpredictable and life‐threatening bleeding. The prevalence of symptomatic patients is 1 in 300,000. Treatment is mostly given following bleeding, but those with the lowest levels may be offered prophylaxis.
Simon Fletcher +3 more
wiley +1 more source
A Rare Case of Possible Iron Overload and B12 Deficiency in Autoimmune Polyglandular Syndrome Type 3B. [PDF]
Kyan K, Kumar R, Craig D.
europepmc +1 more source

