Beckwith-Wiedemann syndrome (BWS) is a rare genetic overgrowth disorder. It is characterized by a wide spectrum of symptoms and physical findings that vary in range and severity from case to case. However, in many individuals, associated features ...

Beckwith-Wiedemann Syndrome (BWS) is a rare genetic disorder that affects the growth and development of a child. It is characterized by overgrowth of certain parts of the body, including the head, abdomen, and extremities. Other features of BWS ma...

Beckwith-Wiedemann syndrome (BWS) is a genetic disorder caused by a microdeletion of the 11p15 region of the genome. It is characterized by overgrowth of certain parts of the body, including the tongue, abdominal organs, and other tissues. It is a...

Beckwith-Wiedemann syndrome (BWS) is a genetic disorder caused by a microduplication of the 11p15 region of the genome. It is characterized by overgrowth of the body, abdominal wall defects, and an increased risk of certain types of cancer. BWS is...

Beckwith-Wiedemann syndrome (BWS) is a genetic disorder caused by a genetic abnormality in the 11p15 region of the genome. This abnormality can be due to a translocation, inversion, or other structural rearrangement of the 11p15 region. BWS is cha...

Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder caused by a mutation in the CDKN1C gene. It is characterized by overgrowth of certain parts of the body, including the tongue, abdominal organs, and other tissues. It can also cause a va...

Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder caused by an imprinting defect of the 11p15 region of the genome. It is characterized by overgrowth of certain parts of the body, including the tongue, abdominal organs, and other body p...

Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder caused by a mutation in the NSD1 gene. It is characterized by overgrowth of certain parts of the body, including the tongue, abdominal organs, and/or extremities. Other features of BWS i...

Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder caused by a genetic abnormality in which a person has two copies of chromosome 11 from their father, instead of one copy from each parent. This is known as paternal uniparental disomy of...

Beemer-Ertbruggen syndrome is a rare genetic disorder characterized by intellectual disability, facial dysmorphism, and skeletal abnormalities. It is caused by a mutation in the PIGV gene. Symptoms may include delayed development, low muscle tone,...

Behcet's Disease is a rare, chronic, inflammatory disorder that affects the blood vessels throughout the body. It is characterized by recurrent episodes of inflammation in the mouth, eyes, skin, and joints. It can also cause inflammation of the br...

Behcet's Syndrome is a rare autoimmune disorder that causes inflammation in the blood vessels throughout the body. Symptoms can include mouth and genital ulcers, skin rashes, eye inflammation, and joint pain. It is most common in the Middle East, ...

Bejel, also known as endemic syphilis, is a chronic, sexually transmitted infection caused by the bacterium Treponema pallidum. It is most commonly found in parts of Africa, the Middle East, and Asia. Symptoms of bejel include skin lesions, fever,...

Bell's palsy (Bell palsy) is paralysis of the facial nerve of unknown cause. The diagnosis is made when no other cause can be identified. Although Bell's palsy is thought to be caused by a viral infection of the facial nerve, this hasn't been prov...

Bell's Palsy is a type of facial paralysis that results in the inability to control facial muscles on one side of the face. It is caused by damage or trauma to the facial nerve, which controls the muscles in the face. Symptoms of Bell's Palsy incl...

Bell's Palsy is a form of facial paralysis that results in the inability to control the facial muscles on one side of the face. It is caused by damage or trauma to the facial nerve, which controls the muscles in the face. Symptoms of Bell's Palsy ...