Medizinische Universität Graz - Research portal
Selected Publication:
Haeusler, MC; Ryan, G; Sams, V; Robson, SC; Young, M; Sullivan, ID; Lipitz, S; Rodeck, CH.
Unusual lymphangioma observed prenatally in a 45,X fetus.
Am J Med Genet. 1993; 45(4):508-510
Doi: 10.1002/ajmg.1320450421
(- Case Report)
Web of Science
PubMed
FullText
FullText_MUG
- Leading authors Med Uni Graz
- Haeusler Martin
- Altmetrics:
- Dimensions Citations:
- Plum Analytics:
- Scite (citation analytics):
- Abstract:
- We present a case of a large frontal lesion, suspected on antenatal ultrasound to be a cephalocele. The cardiac anatomy was abnormal and fetal blood sampling showed a 45,X chromosome constitution. Postmortem examination proved this to be a lymphangioma and confirmed the presence of a cardiac defect. We suggest that this lymphangioma represents an unusual manifestation of monosomy X and discuss the importance of doing chromosome analysis in the presence of such a lesion which is of similar appearance as a cephalocele.
- Find related publications in this database (using NLM MeSH Indexing)
- Adult -
- Female -
- Fetal Diseases - diagnosis Fetal Diseases - genetics Fetal Diseases - pathology Fetal Diseases - ultrasonography
- Humans -
- Lymphangioma - diagnosis Lymphangioma - genetics Lymphangioma - pathology Lymphangioma - ultrasonography
- Monosomy -
- Pregnancy -
- Prenatal Diagnosis -
- Scalp -
- Skin Neoplasms - diagnosis Skin Neoplasms - genetics Skin Neoplasms - pathology Skin Neoplasms - ultrasonography
- X Chromosome -
- Find related publications in this database (Keywords)
- TURNER SYNDROME
- MONOSOMY-X, LYMPHATIC TUMORS
- PRENATAL DIAGNOSIS
- FETAL ANOMALIES