Pericallosal lipoma in an infant with fetal alcohol syndrome: a case report

In this article we report a case of pericallosal lipoma in a newborn with fetal alcohol syndrome, brain malformation (agenesis of the corpus callosum), and intrauterine infection (meningitis) diagnosed in a perinatal center.

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Dental and Facial Characteristics of a Patient with Fetal Alcohol Syndrome – Case Report

Dental and Medical Problems ◽

10.17219/dmp/59586 ◽

2015 ◽

Vol 52 (4) ◽

pp. 505-511

Author(s):

Barbara Obłoj ◽

Justyna Sędkiewicz ◽

Katarzyna Ludwików

Keyword(s):

Case Report ◽

Fetal Alcohol Syndrome ◽

Fetal Alcohol

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Evaluation of Corpus Callosum Anisotropy in Young Adults With Fetal Alcohol Syndrome According to Diffusion Tensor Imaging

Alcoholism Clinical and Experimental Research ◽

10.1097/01.alc.0000171934.22755.6d ◽

2005 ◽

Vol 29 (7) ◽

pp. 1214-1222 ◽

Cited By ~ 81

Author(s):

Xiangyang Ma ◽

Claire D. Coles ◽

Mary Ellen Lynch ◽

Stephen M. LaConte ◽

Omar Zurkiya ◽

...

Keyword(s):

Young Adults ◽

Diffusion Tensor Imaging ◽

Corpus Callosum ◽

Fetal Alcohol Syndrome ◽

Diffusion Tensor ◽

Fetal Alcohol

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The fetal alcohol syndrome (FAS): A clinical case report

Pharmacological Research ◽

10.1016/1043-6618(92)90867-b ◽

1992 ◽

Vol 26 ◽

pp. 78

Author(s):

Amalia Scotto di Tella ◽

Giovanna Venturino ◽

Domenico Infuso ◽

Ugo Aiezza ◽

Giovanni D'Amiano

Keyword(s):

Case Report ◽

Fetal Alcohol Syndrome ◽

Clinical Case ◽

Fetal Alcohol

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The Fetal Alcohol Syndrome and Neuroblastoma

PEDIATRICS ◽

10.1542/peds.66.1.130 ◽

1980 ◽

Vol 66 (1) ◽

pp. 130-132

Author(s):

Hannah Kinney ◽

Roger Faix ◽

Jane Brazy

Keyword(s):

Case Report ◽

Neural Crest ◽

Fetal Alcohol Syndrome ◽

Diaphragmatic Hernia ◽

Congenital Anomalies ◽

Adrenal Carcinoma ◽

Multiple Congenital Anomalies ◽

Fetal Alcohol ◽

Neural Crest Tumors

In 1977 Hornstein et al1 reported the occurrence of adrenal carcinoma in a child with fetal alcohol syndrome. Recently Seeler et al2 noted a ganglioneuroblastoma in a child with fetal hydantoin-alcohol syndromes. The association of neural crest tumors with fetal hydantoin syndrome now appears established.2 The following case suggests an association with neoplasia may also exist for fetal alcohol syndrome. CASE REPORT Clinical Summary T.E. was the 1,360 gm product of a 35-week gestation born to a 30-year old, black primigravida. At 11 days of age the patient was transferred to Duke Hospital for evaluation of multiple congenital anomalies and repair of a right-sided diaphragmatic hernia.

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Fetal alcohol syndrome: case report and review of the literature

Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology ◽

10.1016/j.tripleo.2006.09.016 ◽

2007 ◽

Vol 103 (3) ◽

pp. e20-e25 ◽

Cited By ~ 8

Author(s):

Anut Itthagarun ◽

Raj G. Nair ◽

Joel B. Epstein ◽

Nigel M. King

Keyword(s):

Case Report ◽

Fetal Alcohol Syndrome ◽

Review Of The Literature ◽

Fetal Alcohol

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A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia

Journal of Pediatric Genetics ◽

10.1055/s-0040-1712916 ◽

2020 ◽

Author(s):

Tibor Kalmár ◽

Katalin Szakszon ◽

Zoltán Maróti ◽

Alíz Zimmermann ◽

Adrienn Máté ◽

...

Keyword(s):

Case Report ◽

Genetic Testing ◽

Corpus Callosum ◽

Exome Sequencing ◽

Gene Mutations ◽

Brain Malformation ◽

Pontocerebellar Hypoplasia ◽

Gene Set ◽

Corpus Callosum Agenesis

AbstractMicrolissencephaly is a brain malformation characterized by microcephaly and extremely simplified gyral pattern. It may be associated with corpus callosum agenesis and pontocerebellar hypoplasia. In this case report, we described two siblings, a boy and a girl, with this complex brain malformation and lack of any development. In the girl, exome sequencing of a gene set representing 4,813 genes revealed a homozygous AG deletion in exon 7 of the WDR81 gene, leading to a frameshift (c.4668_4669delAG, p.Gly1557AspfsTer16). The parents were heterozygous for this mutation. The boy died without proper genetic testing. Our findings expand the phenotypic and genotypic spectrum of WDR81 gene mutations.

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