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Cutis marmorata telangiectatica congenita (CMTC) is a rare congenital vascular disorder that usually manifests in affecting the blood vessels of the skin. The condition was first recognized and described in 1922 by Cato van Lohuizen, [2] a Dutch pediatrician whose name was later adopted in the other common name used to describe the condition – Van Lohuizen syndrome.
This disorder was recognized as a distinct syndrome in 1997 and named macrocephaly-cutis marmorata telangiectasia congenita or M-CMTC. [12] [13] A new name, macrocephaly-capillary malformation, abbreviated M-CM, was recommended in 2007. [14] This new name was chosen to more accurately describe the skin markings associated with this disorder.
Cutis marmorata (from Latin marmor, "marble") is a benign skin condition which, if persistent, occurs in Cornelia de Lange syndrome, trisomy 13 and trisomy 18 syndromes. [1] When a newborn infant is exposed to low environmental temperatures, an evanescent , lacy, reticulated red and/or blue cutaneous vascular pattern appears over most of the ...
Aplasia cutis congenita (cutis aplasia, congenital absence of skin, congenital scars) Arteriovenous fistula; Benign neonatal hemangiomatosis; Branchial cyst (branchial cleft cyst) Bronchogenic cyst; Capillary hemangioma (infantile hemangioma, nevus maternus, strawberry hemangioma, strawberry nevus) Cavernous venous malformation
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Type 1 PWS + epidermal nevus; Type 2 (most common): PWS + dermal melanocytosis +/- nevus anemicus; Type 3: PWS + nevus spilus +/- nevus anemicus; Type 4: PWS + nevus spilus + dermal melanocytosis +/- nevus anemicus; Type 5: CMTC (Cutis marmorata telangiectatica congenita) + dermal melanocytosis; They all can contain capillary malformation.
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Diffuse capillary malformation with overgrowth (DCMO) is a subset of capillary malformations (CM) associated with hypertrophy, i.e. increased size of body structures.CM can be considered an umbrella term for various vascular anomalies caused by increased diameter or number of capillary blood vessels.