Results 101 to 110 of about 491,144 (249)

Recurrent bilateral cystic hygroma of the submandibular space in an adult patient

Saudi Journal of Oral Sciences, 2015
Cystic hygroma is an uncommon type of benign neoplasm of lymphangioma commonly seen in children, rarely reported in adults. Most of the cases occur in head and neck region. The etiology and pathogenesis of this entity are still unclear.
Vijayalakshmi S Kotrashetti, Sharadindu M Kotrashetti   +1 more
doaj   +1 more source

VASCULAR LYMPHATIC MALFORMATION WITH UNCOMMON LOCALIZATION [PDF]

, 2016
Introdução: As malformações vasculares linfáticas são entidades raras que afetam os vasos linfáticos. Os autores relatam um caso clínico de uma malformação linfática abdomino-pélvica. Caso Clínico: 28 anos, Gesta 2, Para 1.
Carmo, Olímpia, Inocêncio, Gonçalo, Moreira, Madalena, Oliveira, Luísa, Rodrigues, Ana Isabel, Rodrigues, Graça, Rodrigues, Maria do Céu, Vieira, Alberto, Yida, Fan   +8 more
core  

Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity [PDF]

, 2003
Background Wolf-Hirschhorn syndrome is caused by distal deletion of the short arm of chromosome 4 (4p-). We report a case in which intrauterine growth restriction, hypospadias and foot deformity were detected by prenatal ultrasound examination at 29 ...
Ermis Hayri, Basaran Seher, Karaca Nilay, Aslan Halil, Ceylan Yavuz   +4 more
core   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Chronic subdural haematoma and arachnoid cyst in autosomal dominant polycystic kidney disease (ADPKD) [PDF]

, 2005
We present the unusual association between chronic subdural haematoma (CSDH), intracranial arachnoid cyst and autosomal dominant polycystic kidney disease (ADPKD) in a 27-year-old man. CSDH is a documented complication of intracranial arachnoid cyst, the
Leung, GKK, Yiu, WF
core   +1 more source

Surgical Management of Pediatric Lymphatic Malformations: A Cross‐Sectional Study of Outcomes, Complications, and Recurrence at a Tertiary Care Center

Health Science Reports, Volume 9, Issue 3, March 2026.
ABSTRACT Background and Aims Lymphatic malformations (LMs) are congenital anomalies of the lymphatic system, frequently affecting pediatric populations. While complete surgical excision remains a primary therapeutic option, factors influencing outcomes, including lesion location and age at intervention, remain inadequately explored.
Nashwa Mohammed Al Nwaijie, Ahmad Alkheder, Adel Azar, Basem Alarsan Alyaseen, Abdulmajeed Yousfan   +4 more
wiley   +1 more source

Unusual Presentation of Cystic Hygroma in an Adult Patient: A Case Report [PDF]

International Journal of Anatomy Radiology and Surgery
Cystic hygroma is a benign congenital malformation of the lymphatic system that occurs in children less than two years of age. Most of the recognised cases are seen in childhood (80 to 90%) and its presentation in adults is very rare, however, it should ...
Visar Linyu, Kewecho Akami, Marizela J.D.C Carvalho, Shikha Prabhu Lawande, Moameren   +4 more
doaj   +1 more source

Clinical Utility of Prenatal cfDNA Screening for Sex Chromosome Aneuploidies: A Single Center Experience

Molecular Genetics &Genomic Medicine, Volume 14, Issue 3, March 2026.
CfDNA screening effectively detected SCAs often undetected by routine prenatal ultrasound. Maternal SCAs showed rare fetal transmission. ABSTRACT Introduction To assess the clinical efficacy of prenatal cfDNA screening for detecting sex chromosome aneuploidies (SCAs).
Ying Lin, Qun Lu, Yun Wu, Hang Li, Haoyang Feng, Chunyu Luo, Ping Hu, Dong Liang, Zhengfeng Xu   +8 more
wiley   +1 more source

Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural [PDF]

, 2004
Vascular anomalies are divided into tumours and malformations. Haemangiomas are the most frequent amongst the former. Not normally present at birth, except in a premonitory form, they grow for 10-12 months due to hyperplasia, to subsequently undergo ...
Redondo, P. (Pedro)
core  

First Prenatal Diagnosis of a Niemann–Pick Disease Type C2 Revealed by a Cystic Hygroma: A Case Report and Review of the Literature

Frontiers in Endocrinology, 2018
Background The importance of fetal nuchal translucency was highlighted in the early 1990s as a useful first-trimester marker to identify fetal chromosomal abnormalities.
L. Pleș, R. Sima, F. Nedelea, M. Moga
semanticscholar   +1 more source