The ongoing shift toward automation and artificial intelligence (AI) technologies is rapidly reshaping the modern workforce. There’s a popular misconception that AI is merely a tech shift when, in reality, it’s largely a talent shift now required for most businesses to leverage Read More >>>>

B2C and B2-B businesses can build brand awareness through Facebook marketing. The trick is knowing which of Facebook’s many free and paid options are best for your company—and finding the right audience. This comprehensive guide to effective Facebook marketing will Read More >>>>

Bronchiolitis obliterans organizing pneumonia (BOOP) is a rare inflammatory form of idiopathic diffuse interstitial lung disorder that was first described in the 1980s as a unique disease entity composed of clinical symptoms such as flu-like illness in many individuals as Read More >>>>

Branchiootorenal spectrum disorders are inherited as autosomal dominant genetic conditions characterized by malformations of the outer, middle, and inner ear associated with conductive, sensorineural, or mixed hearing impairment, branchial fistulae, cysts, and renal malformations ranging from mild renal hypoplasia to Read More >>>>

Genetics is the scientific study of genes and heredity—of how certain qualities or traits are passed from parents to offspring as a result of changes in DNA sequence. A gene is a segment of DNA that contains instructions for building one Read More >>>>

Branch-oculo-facial syndrome (BOFS) is a rare genetic autosomal dominant multiple-malformation congenital disorder with defects of the head and neck facies, growth retardation, imperforate nasolacrimal duct, and premature aging that are apparent at birth (congenital) and characterized by branchial (cervical or Read More >>>>

Bowenoid Papulosis is a rare, uncommon sexually transmitted cutaneous condition that occurs in both males and females and causes thought to be caused by human papillomavirus type 16 characterized by multiple well-demarcated red-brown to violaceous papules in the genital area Read More >>>>

Bowen Hutterite syndrome is a rare genetic lethal autosomal recessive disorder characterized by distinctive malformations of the head and facial (craniofacial) area as well as additional skeletal, genital, kidney (renal), and/or brain abnormalities that are apparent at birth (congenital). Characteristic Read More >>>>

Bowen disease is a rare chronic atypical slowly progressive epithelial proliferation in-situ squamous cell carcinoma (SCC) of epidermis skin disorder characterized by multiple well-demarcated red-brown to violaceous papules in the genital area. The major etiological factors of BD include ultraviolet Read More >>>>

Bosma arhinia microphthalmia (BAM) syndrome is an extremely rare genetic congenital disorder characterized by severe hypoplasia of the nose and eyes, palatal abnormalities, deficient taste and smell, inguinal hernias, hypogonadotropic hypogonadism with cryptorchidism, bilateral colobomatous microphthalmia, arhinia, high arched palate, Read More >>>>

Börjeson-Forssman-Lehmann syndrome (BFLS) is an extremely rare X-linked recessive intellectual disability (ID) disorder characterized by mutations in the PHF6 gene and characterized by variable cognitive impairment, a distinct facial gestalt, obesity, and hypogonadism, intellectual disability, obesity, seizures, failure of the Read More >>>>

Boring-Opitz syndrome (BOS) is a rare, multiple anomaly syndrome that has distinctive facial features and posture, growth failure, variable but usually severe intellectual disability, and variable anomalies. The facial features may include microcephaly or trigonocephaly / prominent (but not fused) Read More >>>>