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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.
Macrocephaly-cutis marmorata telangiectatica congenita syndrome, Megalencephaly-cutis marmorata telangiectatica congenita syndrome: A newborn child with M-CM syndrome. A port-wine stain is visible under the nose. On the right side of a cheek, capillary malformations are present.
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 ...
DCMO is a unique entity from previously described vascular syndromes including: Klippel–Trenaunay syndrome, macrocephaly-capillary malformation syndrome , cutis marmorata telangiectatica congenita, CLOVES syndrome and Proteus syndrome.
A number of conditions may cause the appearance of livedo reticularis: Cutis marmorata telangiectatica congenita, a rare congenital condition; Sneddon syndrome – association of livedoid vasculitis and systemic vascular disorders, such as strokes, due to underlying genetic cause [6]
Type 5: CMTC (Cutis marmorata telangiectatica congenita) + dermal melanocytosis They all can contain capillary malformation. Type 2 is the most common and can be associated with granular cell tumor.
Cutis marmorata telangiectatica congenita, a rare congenital vascular disorder often affecting the skin first described by Cato van Lohuizen. Central del Movimiento de Trabajadores Costarricenses, a trade union centre in Costa Rica; Cytoplasmic Microtubule Complex, the network of microtubules within the cytoplasm of a cell.
Cutis marmorata telangiectatica congenita (congenital generalized phlebectasia, Van Lohuizen syndrome) Dermal dendrocyte hamartoma Dermatofibroma (benign fibrous histiocytoma, dermal dendrocytoma, fibrous dermatofibroma, fibrous histiocytoma, fibroma simplex, histiocytoma, nodular subepidermal fibrosis, sclerosing hemangioma)