Considerations for Treating Women With HAE: Lessons From a Puzzling Type 3 Case
There are a few considerations that physicians need to make when caring for female patients with HAE-C1INH type I or II or HAE-nl-C1INH.
There are a few considerations that physicians need to make when caring for female patients with HAE-C1INH type I or II or HAE-nl-C1INH.
An updated set of clinical practice guidelines has been issued for the diagnosis and treatment of idiopathic pulmonary fibrosis in adults.
The diagnosis of systemic mastocytosis is particularly challenging when cutaneous symptoms are absent.
Funding for sickle cell disease clinical trials and drug development has steadily increased and groundbreaking gene therapy research is being conducted.
Multiple sclerosis (MS) is the most common immune-mediated demyelinating disease of the central nervous system (CNS). It is also characterized by inflammation and axonal degeneration in the CNS and is vastly heterogeneous in its presentation.1 Diagnosis of MS has improved over time; however, there is still room for improvement: the mean time from first medical…
Duchenne muscular dystrophy (DMD) is a severe, X-linked recessive dystrophinopathy caused by mutations to the DMD gene which results in abnormal dystrophin production.1,2 The mainstay of pharmacologic therapy in patients with DMD is corticosteroid treatment, which is associated with improved survival, cardiovascular and orthopedic outcomes, motor function, strength, and pulmonary function.3,4 DMD is a devastating…