Cutis marmorata telangiectatica congenita is characterized by reticular erythema that is either generalized over the entire body or localized to a specific area or. Cutis marmorata telangiectatica congenita (CMTC) is a rare condition that causes a marbled pattern on the skin. Learn the symptoms, other. Cutis marmorata telangiectatica congenita. Authoritative facts about the skin from DermNet New Zealand Trust.

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Cutis marmorata telangiectatica congenita CMTC is a rare, deep purple, marble- or net-like birthmark. Macrocephaly-cutis marmorata telangiectatica congenita without cutis marmorata? Standard ophthalmologic examination in all cases of CMTC seems unnecessary and should be limited to the cases in which there are vascular lesions around the eyes.

Cutis marmorata telangiectatica congenita – Wikipedia

The Galeazzi sign flexing the hips and knees while the patient is supine to reveal a discrepancy in femur length showed symmetrical knee height. Additional information Further information on this disease Classification s 3 Gene s 0 Clinical signs and symptoms Other website s 4. During the follow-up, there was no visible neurological damage and the seizures did not return.

The 2 children did not show psychomotor or mental retardation. Symptoms of the following disorders can be similar to those of CMTC. Hypoplasia was observed in 8 cases, hyperplasia in 5 cases, and both in 2 cases.


Cutis marmorata telangiectatica congenita

Improvement of the mottled, vascular pattern is usually observed within 2 years. Garzon MC, Schweiger E.

Cutis marmorata telangiectatica congenita. The lesions usually involve an extremity and are associated with a poor prognosis because of the frequent occurrence of thrombosis, bleeding, ulceration, infection, and gangrene. Researchers believe that the disease results relangiectatica genetic mosaicism. The prognosis is favorable in most patients with an isolated cutaneous abnormality. CMTC may appear indented due to dermal atrophy loss of dermis.

Cutis marmorata telangiectatica congenita. Health care resources for this disease Expert centres 56 Diagnostic tests 1 Patient organisations 6 Orphan drug s 0. Cutis marmorata telangiectatica congenita and extensive mongolian spots: Cutis marmorata telangiectatica congenita is present at birth. Boston Children’s Hospital has been named the 1 children’s hospital in the nation by U. Neurologic abnormalities have been reported in maarmorata with cutis marmorata telangiectatica congenita.

Rare Disease Database

CMTC poses little health risk and rarely needs to be treated; less than one percent of children who have CMTC receive any treatment for it. Follow-up visits should include continued screening for associated anomalies and further attempts to rule out the conditions that may initially mimic cutis marmorata telangiectatica congenita.

Br J of Dermatol. A 1-day-old girl with lesions of cutis marmorata telangiectatica congenita that resemble nevi flammei. The prognosis of CMTC is good. We examined the extent and the distribution of the CMTC lesions, the associated anomalies, the features, and the observations that were recorded during the follow-up.


In the present study, we observed a rapid improvement of the skin lesions within 2 years either leading to a total disappearance of the lesions or markedly improved residual lesions, a finding that agrees with those of other studies. We studied the medical records of 35 patients who were seen at the Pediatric Dermatology Unit of the Sophia Children’s Hospital in Rotterdam, the Netherlands, between July and February Cutis marmorata telangiectatica congenita: The diagnosis of Adams-Oliver syndrome was suspected in 1 patient who had aplasia cutis congenita of the scalp along with syndactyly digits 2 and 3 of both feet.

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Cutis Marmorata Telangiectatica Congenita – NORD (National Organization for Rare Disorders)

Information on current clinical trials congenitq posted on the Internet at www. Aside from dermal melanocytosis patches of hyperpigmentationcutaneous lesions were absent from other areas of the skin, including the head and neck region. Get free access to newly published articles. The main features of Adams—Oliver syndrome are:.

Gerritsen MJ, et al. Cutis marmorata telangiectasia congenita. Author information Copyright and License information Disclaimer. Giuliano F, et al.