Literature DB >> 29541808

Fowler syndrome and fetal MRI findings: a genetic disorder mimicking hydranencephaly/hydrocephalus.

Beth M Kline-Fath1,2, Arnold C Merrow3,4, Maria A Calvo-Garcia3,4, Usha D Nagaraj3,4, Howard M Saal4,5.   

Abstract

Fetal ventriculomegaly is a common referral for prenatal MRI, with possible etiologies being hydrocephalus and hydranencephaly. The underlying cause of hydranencephaly is unknown, but many have suggested that the characteristic supratentorial injury is related to idiopathic bilateral occlusions of the internal carotid arteries from an acquired or destructive event. Fowler syndrome is a rare genetic disorder that causes fetal akinesia and a proliferative vasculopathy that can result in an apparent hydranencephaly-hydrocephaly complex. On prenatal imaging, the presence of significant parenchymal loss in the supratentorial and infratentorial brain is a clue to the diagnosis, which should prompt early genetic testing.

Entities:  

Keywords:  Fetus; Fowler syndrome; Hydranencephaly; Hydrocephalus; Magnetic resonance imaging

Mesh:

Year:  2018        PMID: 29541808     DOI: 10.1007/s00247-018-4106-z

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  8 in total

1.  Congenital hydrocephalus-hydrencephaly in five siblings, with autopsy studies: a new disease.

Authors:  M Fowler; R Dow; T A White; C H Greer
Journal:  Dev Med Child Neurol       Date:  1972-04       Impact factor: 5.449

2.  Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome).

Authors:  Esther Meyer; Christopher Ricketts; Neil V Morgan; Mark R Morris; Shanaz Pasha; Louise J Tee; Fatimah Rahman; Anne Bazin; Bettina Bessières; Pierre Déchelotte; Mohamed T Yacoubi; Mudher Al-Adnani; Tamas Marton; David Tannahill; Richard C Trembath; Catherine Fallet-Bianco; Phillip Cox; Denise Williams; Eamonn R Maher
Journal:  Am J Hum Genet       Date:  2010-03-04       Impact factor: 11.025

3.  The Fowler syndrome-associated protein FLVCR2 is an importer of heme.

Authors:  Simon P Duffy; Jennifer Shing; Punit Saraon; Lloyd C Berger; Maribeth V Eiden; Andrew Wilde; Chetankumar S Tailor
Journal:  Mol Cell Biol       Date:  2010-09-07       Impact factor: 4.272

4.  High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy.

Authors:  Sophie Thomas; Ferechté Encha-Razavi; Louise Devisme; Heather Etchevers; Bettina Bessieres-Grattagliano; Géraldine Goudefroye; Nadia Elkhartoufi; Emilie Pateau; Amale Ichkou; Maryse Bonnière; Pascale Marcorelle; Philippe Parent; Sylvie Manouvrier; Muriel Holder; Annie Laquerrière; Laurence Loeuillet; Joelle Roume; Jelena Martinovic; Soumaya Mougou-Zerelli; Marie Gonzales; Vincent Meyer; Marc Wessner; Christine Bole Feysot; Patrick Nitschke; Nadia Leticee; Arnold Munnich; Stanislas Lyonnet; Peter Wookey; Gabor Gyapay; Bernard Foliguet; Michel Vekemans; Tania Attié-Bitach
Journal:  Hum Mutat       Date:  2010-10       Impact factor: 4.878

5.  Fowler syndrome-a clinical, radiological, and pathological study of 14 cases.

Authors:  Denise Williams; Chirag Patel; Catherine Fallet-Bianco; Karthik Kalyanasundaram; Mohamed Yacoubi; Pierre Déchelotte; Rosemary Scott; Anne Bazin; Bettina Bessières; Tamas Marton; Phillip Cox
Journal:  Am J Med Genet A       Date:  2010-01       Impact factor: 2.802

6.  Looking at the missing brain: hydranencephaly case series and literature review.

Authors:  Giovanni Cecchetto; Laura Milanese; Renzo Giordano; Alessia Viero; Vincenzo Suma; Renzo Manara
Journal:  Pediatr Neurol       Date:  2013-02       Impact factor: 3.372

7.  Fowler syndrome presenting as a Dandy-Walker malformation: a second case report.

Authors:  Mudher Al-Adnani; Liina Kiho; Irene Scheimberg
Journal:  Pediatr Dev Pathol       Date:  2009 Jan-Feb

Review 8.  Hydranencephaly: cerebral spinal fluid instead of cerebral mantles.

Authors:  Piero Pavone; Andrea D Praticò; Giovanna Vitaliti; Martino Ruggieri; Renata Rizzo; Enrico Parano; Lorenzo Pavone; Giuseppe Pero; Raffaele Falsaperla
Journal:  Ital J Pediatr       Date:  2014-10-18       Impact factor: 2.638

  8 in total

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