Results 31 to 40 of about 2,039 (202)

CUTIS MARMORATA TELANGIECTATICA CONGENITA: A CASE REPORT

open access: hybridPreventive Paediatrics, 2023
Introduction: A very rare congenital vascular malformation − Cutis marmorata telangiectatica congenita, also known as Van Lohuizen syndrome is characterised by the presence of a bluish-violet reticulated.
Gordana Đorđević   +4 more
semanticscholar   +3 more sources

Cutis marmorata telangiectatica congenita with skin ulceration: a rare benign skin vascular malformation. [PDF]

open access: yesBMJ Case Rep, 2018
Cutis marmorata telangiectatica congenita (CMTC) is a sporadic congenital disorder characterised by localised or generalised cutaneous vascular anomaly.
Jia D, Rajadurai VS, Chandran S.
europepmc   +2 more sources

Infrequent associations of cutis marmorata telangiectatica congenita: a two-case report.

open access: bronzeCirugía pediátrica
INTRODUCTION Cutis marmorata telangiectatica congenita (CMTC) is a rare capillary malformation characterized by persistent reticular and violaceous erythema. We present two cases of CMTC. CLINICAL OBSERVATION The first case involved a 13-month-old male
JC Moreno Alfonso   +2 more
semanticscholar   +2 more sources

1293 The effectiveness of cutis marmorata telangiectatica congenita laser therapy [PDF]

open access: bronzeJournal of Investigative Dermatology, 2023
A. Mataczynska   +3 more
semanticscholar   +2 more sources

Ossification in Normal and Pathological Contexts: The Key Role of Static Osteogenesis vs. Dynamic Osteogenesis in the Etiopathology of Some Skeletal Alterations. [PDF]

open access: yesBiomolecules
This Commentary is intended to start a discussion in the field of calcification/ossification related to osteogenesis. It highlights that two types of bone formation, static osteogenesis (SO) and dynamic osteogenesis (DO), are temporally followed by each ...
Palumbo C, Paganelli F, Ferretti M.
europepmc   +3 more sources

Case Report: A novel DLL4 variant in a neonate with Adams-Oliver syndrome [PDF]

open access: yesFrontiers in Pediatrics
Adams-Oliver syndrome is a rare congenital disorder with six subtypes that have been identified. Subtypes 1, 3, 5, and 6 have an autosomal dominant inheritance pattern, whereas subtypes 2 and 4 have an autosomal recessive inheritance pattern.
Yanping Huang   +4 more
doaj   +2 more sources

RETINAL NEOVASCULARIZATION FROM A PATIENT WITH CUTIS MARMORATA TELANGIECTATICA CONGENITA.

open access: hybridRetinal cases & brief reports, 2018
PURPOSE To report a rare case of peripheral retinal neovascularization in a patient diagnosed with cutis marmorata telangiectatica congenita (CMTC). METHODS Observational case report.
Therese Sassalos   +3 more
semanticscholar   +2 more sources

Macrocephaly with cutis marmorata telangiectatica congenita: Appending a case in literaure

open access: diamondIndian Journal of Paediatric Dermatology, 2016
Macrocephaly with cutis marmorata telangiectatica congenita (M-CMTC) is a cutaneous disorder often accompanied by additional anomalies, most commonly segmental overgrowth.
Swati Mulye   +2 more
doaj   +2 more sources

Cutaneous Features of Adams-Oliver Syndrome: Diagnosis, Differentiation, and Management. [PDF]

open access: yesPediatr Dermatol
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.
europepmc   +2 more sources

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