What does FFDD mean in UNCLASSIFIED
Focal facial dermal dysplasia (FFDD) is an umbrella term used to describe a rare genodermatosis (skin condition) characterized by abnormal growth, development, and structure of the skin due to a genetic mutation. The abnormalities may present in different areas of the body including the face, hands, feet, trunk, limbs and scalp. While the exact cause of FFDD is unknown, it is believed to be related to a mutation that affects either protein production or structural stability of specialized proteins in the skin cells. Most cases are diagnosed in childhood or adolescence with typical signs and symptoms including hyperpigmentation (dark patches on the skin), hypopigmentation (light patches on the skin), thickened areas on or around bones, decreased subcutaneous fat under the skin and nail defects. Treatment usually involves therapies such as laser treatments, chemical peels or topical medications to improve appearance and scarring caused by lesions.
FFDD meaning in Unclassified in Miscellaneous
FFDD mostly used in an acronym Unclassified in Category Miscellaneous that means Focal facial dermal dysplasia
Shorthand: FFDD,
Full Form: Focal facial dermal dysplasia
For more information of "Focal facial dermal dysplasia", see the section below.
FFDD Meaning in MISCELLANEOUS
In medical terms, Focal Facial Dermal Dysplasia represents an umbrella term used to describe a rare genodermatosis (skin condition). Its main symptoms include abnormalities that manifest itself differently in different parts of the body like hyperpigmentation, hypopigmentation etc., thus making its diagnosis difficult too. Usually these conditions are diagnosed during childhood or adolescent however treatment options are available ranging from laser treatments, chemical peels or topical medications which help reduce scarring caused by lesions as well.
Essential Questions and Answers on Focal facial dermal dysplasia in "MISCELLANEOUS»UNFILED"
What is focal facial dermal dysplasia?
Focal facial dermal dysplasia (also known as aplasia cutis congenita) is a rare disorder which affects the skin and other tissues of the face. It presents with areas of absent, underdeveloped or abnormally developed tissue in the face at birth or shortly thereafter.
What are the symptoms of focal facial dermal dysplasia?
Symptoms can vary from mild to severe based on the extent of tissue involvement. Common signs include patches of missing hair, smooth pale skin, various lesions such as cysts, pits and dimples, growths and malformations such as overgrowth of bone and cartilage, and abnormalities involving structures such as eyelids, eyes and ears.
Who is at risk for focal facial dermal dysplasia?
This condition is inherited in an autosomal recessive pattern, meaning both parents must carry a mutated gene for their child to be affected by it. But it may also arise spontaneously due to unknown factors.
How is focal facial dermal dysplasia diagnosed?
Diagnosis is often made based on clinical examination and medical history. Genetic testing may be used to confirm the diagnosis and identify which genes are involved.
What treatment options are available for focal facial dermal dysplasia?
Treatment usually includes surgical intervention for any deformities or growths present as well as physical therapy to help improve movement range in affected parts of the face. Reconstructive surgery may also be necessary depending on severity.
Are there any long-term effects associated with focal facial dermal dysplasia?
Depending on severity, some individuals with this condition may experience long-term effects including speech impediments caused by malformation of lips/tongue/mouth AND cognitive deficits resulting from abnormal brain development OR hearing loss caused by outer ear deformity.
Final Words:
Focal facial dermal dysplasia is an umbrella term used for describing a rare genodermatosis (skin condition). It has no set cause yet but is believed to be caused by mutations that affect both protein production as well as their structural stability within skin cells. Its effects manifest differently depending on where it occurs but generally includes features like hyperpigmentation, hypopigmentation etc.. Treatment can range from laser treatments to simple topical medications which can help reduce scarring caused by lesions associated with this syndrome.
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