WordNet

of or relating to the ectoderm (同)ectodermic
abnormal development (of organs or cells) or an abnormal structure resulting from such growth
the outer germ layer that develops into skin and nervous tissue (同)exoderm, ectoblast
a capacity unit used for measuring fresh herring

UpToDate Contents

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1. 遺伝性皮膚症 the genodermatoses
2. 歯の解剖学的構造および発達 anatomy and development of the teeth
3. 小児の不明熱に対するアプローチ fever of unknown origin in children evaluation
4. 複合免疫不全 combined immunodeficiencies
5. 歯の発達障害 developmental defects of the teeth

English Journal

Sensenbrenner syndrome: a new member of the hepatorenal fibrocystic family.

Zaffanello M1, Diomedi-Camassei F, Melzi ML, Torre G, Callea F, Emma F.
American journal of medical genetics. Part A.Am J Med Genet A.2006 Nov 1;140(21):2336-40.
Cranioectodermal dysplasia (CED, Sensenbrenner syndrome; OMIM #218330) is an autosomal recessive disorder reported only in 15 cases, which is characterized by dolichocephaly, rhizomelic dwarfism, dental and nail dysplasia, and progressive tubulo-interstitial nephritis (TIN) leading to end-stage rena
PMID 17022080

[Cranio-ectodermal dysplasia].

Okuyama T1.
Ryōikibetsu shōkōgun shirīzu.Ryoikibetsu Shokogun Shirizu.2001;(33):509-10.
PMID 11462542

[Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report].

Costet C1, Betis F, Bérard E, Tsimaratos M, Sigaudy S, Antignac C, Gastaud P.
Journal français d'ophtalmologie.J Fr Ophtalmol.2000 Feb;23(2):158-60.
PURPOSE: Sensenbrenner syndrome or cranio-ectodermal dysplasia is an extremely rare autosomal recessive condition (12 cases reported in literature). Our observation shows the possibility of both ocular and renal involvement associated with cranio-ectodermal abnormalities.PATIENTS: and method:We repo
PMID 10705117

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