Congenital Yellow Nail Syndrome: A Case Report and Its Relationship to Nonimmune Fetal Hydrops

2010 ◽  
Vol 27 (5) ◽  
pp. 533-534 ◽  
Author(s):  
ARTI NANDA ◽  
FAHAD H. AL-ESSA ◽  
WAEL M. EL-SHAFEI ◽  
QASEM A. ALSALEH
Keyword(s):  
Case Report ◽  
Fetal Hydrops ◽  
Yellow Nail Syndrome

scholarly journals Yellow nail syndrome: a case report

2014 ◽  
Vol 18 (1) ◽  
pp. 680-682 ◽  
Author(s):  
Kawa Hassan
Keyword(s):  
Case Report ◽  
Yellow Nail Syndrome

Perinatal Manifestations of Maternal Yellow Nail Syndrome

PEDIATRICS ◽  
1992 ◽  
Vol 89 (6) ◽  
pp. 1016-1018
Author(s):  
Paul Govaert ◽  
Jules G. Leroy ◽  
Romain Pauwels ◽  
Piet Vanhaesebrouck ◽  
Claudine De Praeter ◽  
...  
Keyword(s):  
Clinical Findings ◽  
Neurological Development ◽  
Fetal Hydrops ◽  
Nail Dystrophy ◽  
Chromosomal Disorders ◽  
Yellow Nail Syndrome ◽  
Nail Changes ◽  
Pulmonary Lymphangiectasis ◽  
Multiple Pterygium Syndrome ◽  
Dystrophic Nail

A term female firstborn infant had unexplained nonimmune fetal hydrops and recurrent left chylothorax at 4 weeks of age. A few months before conception, her mother had had acute dystrophic nail changes and is being treated for recurrent sinusitis, bronchiectasis, and a deficiency of serum IgG2. We suggest that they both suffer from a dominantly inherited congenital lymphedema syndrome known as `yellow nail dystrophy.' Prenatal manifestation of this disorder has not been reported previously. The child's anthropometric and neurological development was normal at 1 year of age, whereas mild ankle edema and marbling of the skin of the limbs were salient clinical findings. Inherited lymphedema leading to nonimmune fetal hydrops also has been recognized in chromosomal disorders, Noonan's syndrome, multiple pterygium syndrome, pulmonary lymphangiectasis, and mixed-vessel lymphatic dysfunction. Indicators of parental lymphedema are not on record in those instances.

Glycogen Storage Disease Presenting as Fetal Hydrops: A Case Report

2013 ◽  
Vol 24 (3) ◽  
pp. 187
Author(s):  
Rimm Huh ◽  
So Yoon Ahn ◽  
Se In Sung ◽  
Hye Su Yoo ◽  
Yeon Lim Seo ◽  
...  
Keyword(s):  
Case Report ◽  
Glycogen Storage Disease ◽  
Storage Disease ◽  
Glycogen Storage ◽  
Fetal Hydrops

Case Report: Fetal Hydrops Associated with Intrauterine Supraventricular Tachycardia

1983 ◽  
Vol 27 (1) ◽  
pp. 37-38 ◽  
Author(s):  
CHRISTINE M. ACTON ◽  
JEREMY N. OATS ◽  
GERALD A. MANLY
Keyword(s):  
Case Report ◽  
Supraventricular Tachycardia ◽  
Fetal Hydrops

Yellow nail syndrome: a case report and review of treatment options

2015 ◽  
Vol 11 (4) ◽  
pp. 405-410 ◽  
Author(s):  
Michael Kurin ◽  
Jonathan Wiesen ◽  
Atul C. Mehta
Keyword(s):  
Case Report ◽  
Treatment Options ◽  
Yellow Nail Syndrome

scholarly journals Galactosialidosis presenting as nonimmune fetal hydrops: a case report

2009 ◽  
Vol 29 (9) ◽  
pp. 895-896 ◽  
Author(s):  
Susana Carvalho ◽  
Márcia Martins ◽  
Ana Fortuna ◽  
Umbelina Ramos ◽  
Carlos Ramos ◽  
...  
Keyword(s):  
Case Report ◽  
Fetal Hydrops

scholarly journals Giant Intrapericardial Teratoma – Enough Space Left in the Neonatal Thorax?

2020 ◽  
pp. 43-46
Author(s):  
Michael Weidenbach ◽  
Christian Paech ◽  
Frauke Hornemann ◽  
Marcel Vollroth
Keyword(s):  
Decision Making ◽  
Case Report ◽  
Continuous Positive Airway Pressure ◽  
Airway Pressure ◽  
Positive Airway Pressure ◽  
Case Reports ◽  
Fetal Hydrops ◽  
Fetal Intervention ◽  
Post Surgery ◽  
Disease Case

Objective: Optimal treatment of fetal intrapericardial teratoma is controversial, especially in regard to fetal intervention. Given the rarity of the disease case reports can assist in decision making. Case Report: We report on a neonate with a giant intrapericardial teratoma detected in utero, almost filling the entire thorax. Delivery was planned per cesarean section with extracorporeal membrane oxygenation (ECMO) stand-by. As a surprise the child adopted very well after birth, requiring only continuous positive airway pressure (CPAP). The tumor was resected on the next day without injuring cardiac structures. The child was and discharged on day 10 post-surgery. Conclusion: Our case supports the assumption that even in very large tumors the postnatal course can be benign, if there is no fetal hydrops.

scholarly journals A Case of Situs Ambiguous and Complex Cardiac Defect Presenting as Fetal Hydrops

2017 ◽  
Vol 02 (02) ◽  
pp. 060-063
Author(s):  
Shagun Aggarwal
Keyword(s):  
Case Report ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
Cardiac Defect ◽  
Fetal Hydrops ◽  
Cardiac Defects ◽  
Live Births ◽  
Situs Ambiguous ◽  
Laterality Defects

AbstractSitus ambiguous comprises of 3% of congenital heart defects and is present in at least 1 in 10,000 live births. Most cases diagnosed prenatally are associated with complex cardiac defects which can be detected by ultrasonography. This is a case report of a fetus presenting with hydrops, which was detected to have situs ambiguous, a complex cardiac defect and multiple laterality defects on autopsy.

Fetal hydrops in GM1 gangliosidosis: A case report

2007 ◽  
Vol 94 (12) ◽  
pp. 1847-1849 ◽  
Author(s):  
Maria Teresa Sinelli ◽  
Mario Motta ◽  
Donatella Cattarelli ◽  
Maria Luisa Cardone ◽  
Gaetano Chirico
Keyword(s):  
Case Report ◽  
Fetal Hydrops ◽  
Gm1 Gangliosidosis
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