Literature DB >> 9354837

Macrocephaly with cutis marmorata, haemangioma and syndactyly--a distinctive overgrowth syndrome.

J Clayton-Smith1, B Kerr, H Brunner, L Tranebjaerg, A Magee, R C Hennekam, R F Mueller, L Brueton, M Super, J Steen-Johnsen, D Donnai.   

Abstract

We describe nine children with a similar pattern of features including macrocephaly and cutis marmorata telangiectatica congenita. All were large at birth and had a distinctive capillary haemangioma involving the philtrum and upper lip. The seven who survived all developed hydrocephalus and had developmental delay. Six developed body asymmetry and three had internal arteriovenous malformations. Syndactyly of the second and third toes and/or the third and fourth fingers or toes was commonly seen. All of the cases were sporadic. This condition is easily recognizable and should be considered in the differential diagnosis of patients presenting with overgrowth and macrocephaly.

Entities:  

Mesh:

Year:  1997        PMID: 9354837     DOI: 10.1097/00019605-199710000-00001

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  22 in total

Review 1.  Approach to the Diagnosis of Overgrowth Syndromes.

Authors:  Mohnish Suri
Journal:  Indian J Pediatr       Date:  2015-12-18       Impact factor: 1.967

2.  The microcephaly-capillary malformation syndrome.

Authors:  Ghayda M Mirzaa; Alex R Paciorkowski; Christopher D Smyser; Marcia C Willing; Anne C Lind; William B Dobyns
Journal:  Am J Med Genet A       Date:  2011-08-03       Impact factor: 2.802

Review 3.  Multifocal arteriovenous malformations and facial nevus without leptomeningeal angioma: a variant form of Sturge-Weber syndrome? A case report and review of the literatures.

Authors:  In-Seok Bae; Hyeong-Joong Yi; Young Jun Lee
Journal:  Childs Nerv Syst       Date:  2012-09-30       Impact factor: 1.475

Review 4.  Clinical review of genetic epileptic encephalopathies.

Authors:  Grace J Noh; Y Jane Tavyev Asher; John M Graham
Journal:  Eur J Med Genet       Date:  2012-01-25       Impact factor: 2.708

5.  Tetralogy of Fallot associated with macrocephaly-capillary malformation syndrome: a case report and review of the literature.

Authors:  Jesus E Dueñas-Arias; Eliakym Arámbula-Meraz; Luis O Frías-Castro; Rosalio Ramos-Payán; Jose A Quibrera-Matienzo; Fred Luque-Ortega; E Maribel Aguilar-Medina
Journal:  J Med Case Rep       Date:  2009-09-08

Review 6.  Neurocutaneous vascular syndromes.

Authors:  Katherine B Puttgen; Doris D M Lin
Journal:  Childs Nerv Syst       Date:  2010-06-27       Impact factor: 1.475

7.  Growth hormone deficiency in megalencephaly-capillary malformation syndrome: An association with activating mutations in PIK3CA.

Authors:  Shanlee Davis; Meredith A Ware; Jordan Zeiger; Matthew A Deardorff; Katheryn Grand; Adda Grimberg; Stephanie Hsu; Megan Kelsey; Shideh Majidi; Revi P Matthew; Melanie Napier; Natalie Nokoff; Chitra Prasad; Andrew C Riggs; Margaret L McKinnon; Ghayda Mirzaa
Journal:  Am J Med Genet A       Date:  2019-11-15       Impact factor: 2.802

Review 8.  Megalencephaly-capillary malformation syndrome and associated hydrocephalus: treatment options and revision of the literature.

Authors:  M Alamar; S Candela; A Flor-Goikoetxea; H Salvador; A F Martinez-Monseny; J Muchart; J Hinojosa
Journal:  Childs Nerv Syst       Date:  2021-05-28       Impact factor: 1.475

9.  Germline PTPN11 and somatic PIK3CA variant in a boy with megalencephaly-capillary malformation syndrome (MCAP)--pure coincidence?

Authors:  Dennis Döcker; Max Schubach; Moritz Menzel; Christiane Spaich; Heinz-Dieter Gabriel; Martin Zenker; Deborah Bartholdi; Saskia Biskup
Journal:  Eur J Hum Genet       Date:  2014-06-18       Impact factor: 4.246

10.  Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.

Authors:  Robert L Conway; Barry D Pressman; William B Dobyns; Moise Danielpour; John Lee; Pedro A Sanchez-Lara; Merlin G Butler; Elaine Zackai; Lindsey Campbell; Sulagna C Saitta; Carol L Clericuzio; Jeff M Milunsky; H Eugene Hoyme; Joseph Shieh; John B Moeschler; Barbara Crandall; Julie L Lauzon; David H Viskochil; Brian Harding; John M Graham
Journal:  Am J Med Genet A       Date:  2007-12-15       Impact factor: 2.802

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