Cutis marmorata telangiectatica congenita: a mimicker of a common disorder. [PDF]
Levy R, Lam JM.
europepmc +2 more sources
Ophthalmologic alterations in cutis marmorata telangiectatica congenita: a series of cases. [PDF]
Makita LS, Muniz BC, Medina FMC.
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Cutaneous neonatal lupus with cutis marmorata telangiectatica congenita-like lesions. [PDF]
Trevisan F +3 more
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Cutis marmorata telangiectatica congenita and aberrant Mongolian spots: Type V phacomatosis pigmentovascularis or phacomatosis cesiomarmorata. [PDF]
Du G, Zhang X, Zhang T.
europepmc +3 more sources
Cutis marmorata telangiectatica congenita
H Mocan +4 more
doaj +2 more sources
Cutaneous Features of Adams-Oliver Syndrome: Diagnosis, Differentiation, and Management. [PDF]
ABSTRACT Adams‐Oliver syndrome (AOS) is a rare genetic disorder primarily characterized by aplasia cutis congenita (ACC) and terminal transverse limb defects. The condition presents with a range of cutaneous features, most notably ACC, cutis marmorata telangiectatica congenita, and nail anomalies.
Yang S, Lam JM.
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Laseroterapia malformacji naczyniowej cutis marmorata telangiectatica congenita [PDF]
The purpose of this study is to determine a long-term effectiveness of a 532 nm and 1064 nm large spot laser with contact cooling in the treatment of CMTC.
Kwiek, Bartłomiej +3 more
core +5 more sources
Cutis marmorata telangiectatica congenita.
J L, Caballero +2 more
+6 more sources
A newborn with a rare association of various congenital skin disorders – Answer
We report a female newborn with a combination of 3 skin lesions: Mongolian spots, port-wine stains, and cutis marmorata telangiectatica congenita. This association is an unclassifiable form of phacomatosis and only 7 similar cases have been published in ...
Federico Mecarini +2 more
doaj +1 more source
An Extremely Preterm Infant With <i>PIK3CA-</i>Related Overgrowth Spectrum (PROS): Alpelisib Treatment and Outcome. [PDF]
Phosphatidylinositol 4,5‐bisphosphate 3‐kinase catalytic subunit alpha (PIK3CA)‐related overgrowth spectrum (PROS) is a group of rare genetic asymmetric and atypical overgrowth disorder syndromes. Affecting skin, adipose and connective tissues, brain, bone, and vasculature and severity influenced by the gestational age at which the change occurred ...
Anderson S, Velinov M.
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