About Craniofrontonasal Syndrome

Craniofrontonasal Syndrome, also known as craniofrontonasal dysplasia, is related to frontonasal dysplasia 1 and hemifacial hyperplasia, and has symptoms including grooving of nail An important gene associated with Craniofrontonasal Syndrome is EFNB1 (Ephrin B1), and among its related pathways/superpathways are Nervous system development and TGF-Beta Pathway. Affiliated tissues include bone, brain and skin, and related phenotypes are frontal bossing and hypertelorism

Major Symptoms of Craniofrontonasal Syndrome

Craniofrontonasal syndrome is a rare autoimmune disorder that affects the nasal passages and sinuses. The major symptoms include recurrent infections, chronic nasal congestion, facial pain and pressure, and a persistent runny nose.

Suitable Lifestyle for People with Craniofrontonasal Syndrome

Craniofrontonasal syndrome (craniofrontal syndrome) is a rare neurodevelopmental disorder characterized by underdevelopment of the prefrontal and parietal lobes, resulting in social, language and cognitive difficulties. However, the condition does not affect the patient's lifestyle. Patients can still enjoy rich life activities such as socializing with others, studying, and traveling. In terms of care, patients require special support and attention to help them overcome life challenges.

Other Diseases

Down Syndrome Dry Eye Syndrome FG Syndrome 3C Syndrome 3-M Syndrome Cat Eye Syndrome KBG Syndrome ICF Syndrome NDH Syndrome H Syndrome

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