Congenital lymphedema is a blockage of fluid in the developing fetal lymphatic system. It is diagnosed by a nuchal scan. Presence of this condition is also associated with congenital heart defect.[1]
See also
References
- ↑ "Relationship Between Nuchal Translucency Thickness and Prevalence of Major Cardiac Defects in Fetuses With Normal Karyotype", by Atzei, A; Gajewska, K; Huggon, I C.; Allan, L; Nicolaides, K H. Obstetrical and Gynecological Survey. January 2006. Volume 61, Issue 1, pages 8-10.
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Skin disease/ genodermatosis | | |
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| Epidermolysis bullosa simplex ( Generalized, Localized, Herpetiformis, Ogna, With muscular dystrophy, With mottled pigmentation)
Junctional epidermolysis bullosa (Gravis, Mitis, Generalized atrophic, Cicatricial, With pyloric atresia)
Epidermolysis bullosa dystrophica ( Dominant, Recessive) |
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Other | |
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Elastic/Connective | |
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Ungrouped cutaneous congenital anomalies | |
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Ungrouped genodermatoses | |
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Decreases | |
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Increases | | general Bruise/Hematoma: Petechia · Purpura · Ecchymosisregional: head ( Epistaxis, Hemoptysis, Intracranial hemorrhage, Hyphema, Subconjunctival hemorrhage) · torso ( Hemothorax, Hemopericardium, Pulmonary hematoma) · abdomen ( Gastrointestinal bleeding, Haemobilia, Hemoperitoneum, Hematocele, Hematosalpinx ) · joint ( Hemarthrosis) |
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Other | |
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