Literature DB >> 18816642

Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome: CNS malformations and seizures may be a component of this disorder.

Zoran S Gucev1, Velibor Tasic, Aleksandra Jancevska, Marina Krstevska Konstantinova, Nada Pop-Jordanova, Zoran Trajkovski, Leslie G Biesecker.   

Abstract

A newborn girl was found to have a massive lymphatic truncal vascular malformation with overlying cutaneous venous anomaly associated with overgrown feet and splayed toes. These manifestations comprise the recently described CLOVE syndrome. She also had cranial asymmetry and developed generalized seizures, which were treated with anticonvulsants. Cranial CT showed encephalomalacia, widening of the ventricles and the sulci, hemimegalencephaly (predominantly white matter) and partial agenesis of corpus callosum. Review of the literature identified several other patients with CLOVE syndrome, some of whom were misdiagnosed as having Proteus syndrome, with strikingly similar manifestations. We conclude that CNS manifestations including hemimegalencephaly, dysgenesis of the corpus callosum, neuronal migration defects, and the consequent seizures, may be an rarely recognized manifestation of CLOVE syndrome. 2008 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2008        PMID: 18816642      PMCID: PMC2819374          DOI: 10.1002/ajmg.a.32515

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  12 in total

1.  Ocular manifestations in Proteus syndrome.

Authors:  I De Becker; D J Gajda; E Gilbert-Barness; M M Cohen
Journal:  Am J Med Genet       Date:  2000-06-19

Review 2.  Reassessment of the Proteus syndrome literature: application of diagnostic criteria to published cases.

Authors:  Joyce T Turner; M Michael Cohen; Leslie G Biesecker
Journal:  Am J Med Genet A       Date:  2004-10-01       Impact factor: 2.802

Review 3.  The challenges of Proteus syndrome: diagnosis and management.

Authors:  Leslie Biesecker
Journal:  Eur J Hum Genet       Date:  2006-08-02       Impact factor: 4.246

4.  Type 2 segmental Cowden disease vs. Proteus syndrome.

Authors:  R Happle
Journal:  Br J Dermatol       Date:  2007-03-28       Impact factor: 9.302

5.  Clinical differentiation between Proteus syndrome and hemihyperplasia: description of a distinct form of hemihyperplasia.

Authors:  L G Biesecker; K F Peters; T N Darling; P Choyke; S Hill; N Schimke; M Cunningham; P Meltzer; M M Cohen
Journal:  Am J Med Genet       Date:  1998-10-02

Review 6.  Elattoproteus syndrome: delineation of an inverse form of Proteus syndrome.

Authors:  R Happle
Journal:  Am J Med Genet       Date:  1999-05-07

Review 7.  Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation.

Authors:  L G Biesecker; R Happle; J B Mulliken; R Weksberg; J M Graham; D L Viljoen; M M Cohen
Journal:  Am J Med Genet       Date:  1999-06-11

8.  Encephalocraniocutaneous lipomatosis and the Proteus syndrome: distinct entities with overlapping manifestations.

Authors:  S McCall; M I Ramzy; J K Curé; G S Pai
Journal:  Am J Med Genet       Date:  1992-07-01

9.  The radiological features of hemimegalencephaly including three cases associated with proteus syndrome.

Authors:  P D Griffiths; R J Welch; D Gardner-Medwin; A Gholkar; V McAllister
Journal:  Neuropediatrics       Date:  1994-06       Impact factor: 1.947

10.  Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patients.

Authors:  Julie C Sapp; Joyce T Turner; Jiddeke M van de Kamp; Fleur S van Dijk; R Brian Lowry; Leslie G Biesecker
Journal:  Am J Med Genet A       Date:  2007-12-15       Impact factor: 2.802

View more
  15 in total

1.  What is your diagnosis?

Authors:  Manuela Panteliades; Claudia Marcia Resende Silva; Bernardo Gontijo
Journal:  An Bras Dermatol       Date:  2016 May-Jun       Impact factor: 1.896

2.  PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia.

Authors:  Laura A Jansen; Ghayda M Mirzaa; Gisele E Ishak; Brian J O'Roak; Joseph B Hiatt; William H Roden; Sonya A Gunter; Susan L Christian; Sarah Collins; Carissa Adams; Jean-Baptiste Rivière; Judith St-Onge; Jeffrey G Ojemann; Jay Shendure; Robert F Hevner; William B Dobyns
Journal:  Brain       Date:  2015-02-25       Impact factor: 13.501

3.  CLOVE Syndrome.

Authors:  Ananthanarayanan Kasinathan; Naveen Sankhyan; Chirag Kamal Ahuja; Pratibha Singhi
Journal:  Indian J Pediatr       Date:  2017-07-28       Impact factor: 1.967

4.  CLOVES Syndrome: Severe Neonatal Presentation.

Authors:  Silvana Acosta; Viviana Torres; María Paulos; Ignacio Cifuentes
Journal:  J Clin Diagn Res       Date:  2017-04-01

Review 5.  Neurocutaneous Manifestations of Genetic Mosaicism.

Authors:  Maurice A M van Steensel
Journal:  J Pediatr Genet       Date:  2015-11-30

Review 6.  Imaging findings of lipomatosis: a comprehensive review.

Authors:  Seray Akcalar; Baris Turkbey; Tuncay Hazirolan; Musturay Karcaaltincaba; Iclal Ocak; Ustun Aydingoz; Erhan Akpinar
Journal:  Jpn J Radiol       Date:  2012-10-10       Impact factor: 2.374

7.  Prenatal diagnosis of CLOVES syndrome confirmed by detection of a mosaic PIK3CA mutation in cultured amniocytes.

Authors:  Lisa T Emrick; Lauren Murphy; Alireza A Shamshirsaz; Rodrigo Ruano; Christopher I Cassady; Liu Liu; Fengqi Chang; V Reid Sutton; Marilyn Li; Ignatia B Van den Veyver
Journal:  Am J Med Genet A       Date:  2014-07-14       Impact factor: 2.802

Review 8.  Nephroblastomatosis or Wilms tumor in a fourth patient with a somatic PIK3CA mutation.

Authors:  Karen W Gripp; Laura Baker; Vinay Kandula; Katrina Conard; Mena Scavina; Joseph A Napoli; Gregory C Griffin; Mihir Thacker; Rachel G Knox; Graeme R Clark; Victoria E R Parker; Robert Semple; Ghayda Mirzaa; Kim M Keppler-Noreuil
Journal:  Am J Med Genet A       Date:  2016-05-18       Impact factor: 2.802

9.  Teaching NeuroImages: CLOVES Syndrome.

Authors:  Meagan Collins; Eric Krochmalnek; Sarah Alsubhi; Myriam Srour
Journal:  Neurology       Date:  2020-12-01       Impact factor: 9.910

10.  A severe and rapidly progressive case of proteus syndrome in a neonate who presented with unilateral hydrocephalus apart from other typical features of the proteus syndrome.

Authors:  Rakesh Kumar; Puja Bhagat
Journal:  J Clin Neonatol       Date:  2012-07
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.