Cutis marmorata telangiectatica congenita

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Cutis marmorata telangiectatica congenita
Synonyms CMTC
Pronounce
Specialty Dermatology
Symptoms Mottled skin, telangiectasia, ulceration
Complications Ulceration, limb asymmetry
Onset At birth
Duration Lifelong
Types N/A
Causes Unknown
Risks
Diagnosis Clinical diagnosis
Differential diagnosis Klippel–Trénaunay syndrome, Sturge–Weber syndrome
Prevention None
Treatment Supportive care
Medication
Prognosis Generally good
Frequency Rare
Deaths N/A


Cutis marmorata telangiectatica congenita (CMTC) is a rare congenital skin disorder. It is characterized by marbled skin with dilated blood vessels, and may be associated with other physical abnormalities.

Symptoms and Signs[edit]

The primary symptom of CMTC is a marbled or lace-like pattern on the skin, caused by dilated blood vessels. This pattern is usually present at birth and may fade over time. Other symptoms may include:

Causes[edit]

The exact cause of CMTC is unknown. It is thought to be a sporadic condition, meaning it occurs in individuals with no history of the disorder in their family. However, some cases have been reported in siblings, suggesting a possible genetic component.

Diagnosis[edit]

Diagnosis of CMTC is primarily based on the characteristic physical findings. In some cases, a skin biopsy may be performed to confirm the diagnosis. Other tests may be done to check for associated abnormalities, such as heart defects or glaucoma.

Treatment[edit]

There is no specific treatment for CMTC. Management of the condition is focused on treating the symptoms and any associated abnormalities. For example, ulcerations may be treated with wound care, and glaucoma may be treated with eye drops or surgery.

Prognosis[edit]

The prognosis for individuals with CMTC varies. In some cases, the skin abnormalities may improve with age. However, individuals with associated abnormalities may have a poorer prognosis.

See also[edit]

References[edit]


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