Difference between revisions of "Congenital lymphedema"

From Self-sufficiency
Jump to: navigation, search
(links with this topic)
 
m (1 revision)
 
(No difference)

Latest revision as of 20:26, 21 September 2010

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

  1. ↑ "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.
Congenital malformations and deformations of integument (Q80-Q82, 757.0-757.3)
Skin disease/
genodermatosis
Ungrouped
Other
Elastic/Connective
Ungrouped cutaneous
congenital anomalies
With OMIM
Without OMIM
Accessory nail of the fifth toe · Arteriovenous fistula · Bronchogenic cyst · Congenital cartilaginous rest of the neck · Congenital hypertrophy of the lateral fold of the hallux · Congenital lip pit · Congenital malformations of the dermatoglyphs · Congenital preauricular fistula · Congenital smooth muscle hamartoma · Cystic lymphatic malformation · Dermoid cyst · Encephalocele · Infantile hemangioma · Malignant pilomatricoma · Median raphe cyst · Melanotic neuroectodermal tumor of infancy · Mongolian spot · Nasal glioma · Nasolacrimal duct cyst · Omphalomesenteric duct cyst · Pilomatricoma · Poland anomaly · PHACE association · Rapidly involuting congenital hemangioma · Rosenthal–Kloepfer syndrome · Rudimentary supernumerary digit · Sinus pericranii · Skin dimple · Superficial lymphatic malformation · Supernumerary nipple · Thyroglossal duct cyst · Verrucous vascular malformation
Ungrouped
genodermatoses
With OMIM
SLC39A4 (Acrodermatitis enteropathica) · ATP2A2 (Acrokeratosis verruciformis) · C20orf42 ( Kindler syndrome) · GNAS (Albright's hereditary osteodystrophy) · FGFR2 (Apert syndrome) · VPS33B (Arthrogryposis–renal dysfunction–cholestasis syndrome) · MRN complex ( Ataxia telangiectasia) · HR (Atrichia with papular lesions) · AIRE (Autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy syndrome)

deletion: 18q deletion syndrome · Angelman syndrome

genetics unknown: Acrogeria · Adams–Oliver syndrome · Adducted thumbs syndrome · Atrophodermia vermiculata

unsorted: Bart syndrome · Bazex–Dupré–Christol syndrome · Bloom syndrome · BIDS syndrome · Cardiofaciocutaneous syndrome · Cartilage–hair hypoplasia · Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome · Chondrodysplasia punctata · Cockayne syndrome · CHILD syndrome · Conradi–Hünermann syndrome · Costello syndrome · Cronkhite–Canada syndrome · Crouzon syndrome · Cutis verticis gyrata · DeSanctis–Cacchione syndrome · Dolichol kinase deficiency · Ectrodactyly–ectodermal dysplasia–cleft syndrome · Focal dermal hypoplasia · Franceschetti–Klein syndrome · Gardner's syndrome · Hallerman–Streiff syndrome · Hay–Wells syndrome · Hereditary sclerosing poikiloderma · IBIDS syndrome · Incontinentia pigmenti achromians · IPEX syndrome · Johanson–Blizzard syndrome · Johnson–McMillin syndrome · Joubert syndrome · Kabuki syndrome · Klippel–Feil syndrome · Lelis syndrome · Lenz–Majewski syndrome · Mandibuloacral dysplasia · Marinesco–Sjögren syndrome · Metageria · Multiple lentigines syndrome · Multiple sulfatase deficiency · Naegeli–Franceschetti–Jadassohn syndrome · Neurofibromatosis (Neurofibromatosis type 1, Neurofibromatosis type 3, Neurofibromatosis type 4, Segmental neurofibromatosis) · Neutral lipid storage disease · Noonan syndrome · Oculocerebrocutaneous syndrome · Oculodentodigital dysplasia · Odonto–Tricho–Ungual–Digital–Palmar syndrome · Oliver–McFarlane syndrome · Pachydermoperiostosis · Peeling skin syndrome · Pfeiffer syndrome · Popliteal pterygium syndrome · Porokeratosis (Porokeratosis palmaris et plantaris disseminata, Craniosynostosis–anal anomalies–porokeratosis syndrome, Disseminated superficial actinic porokeratosis, Disseminated superficial porokeratosis, Linear porokeratosis, Plaque-type porokeratosis, Punctate porokeratosis) · Prader–Willi syndrome · Progeria · Progressive osseous heteroplasia · Progressive symmetric erythrokeratodermia · Proteus syndrome · Rapp–Hodgkin syndrome · Refsum's disease · Restrictive dermopathy · Rhizomelic chondrodysplasia punctata · Rombo syndrome · Rothmund–Thomson syndrome · Rud syndrome · Say syndrome · Scalp–ear–nipple syndrome · Schindler disease · Schinzel–Giedion syndrome · Scleroatrophic syndrome of Huriez · Senter syndrome · Shabbir syndrome · Silver–Russell syndrome · Skin fragility syndrome · Terminal osseous dysplasia with pigmentary defects · Tooth and nail syndrome · Townes–Brocks syndrome · Transient bullous dermolysis of the newborn · Treacher Collins syndrome · Tricho–rhino–phalangeal syndrome · Tuberous sclerosis · Ulnar–mammary syndrome · Van Der Woude syndrome · Von Hippel–Lindau syndrome · Watson syndrome · Werner syndrome · Westerhof syndrome · Whistling syndrome · Wilson–Turner syndrome · Wolf–Hirschhorn syndrome · X-linked recessive chondrodysplasia punctata · Zimmermann–Laband syndrome
Without OMIM

M: INT, SF, LCT

noco(i/b/d/q/u/r/p/m/k/v/f)/cong/tumr(n/e/d), sysi/epon

proc, drug (D2/3/4/5/8/11)

Lymph nodes
Lymph vessels
Decreases
Increases
Other
Retrieved from "http://ssf.f15ijp.com/wiki/index.php?title=Congenital_lymphedema&oldid=38990"