Übersetzung für 'Alagille syndrome' von Englisch nach Deutsch

Alagille syndrome <ALGS>

Alagille-Syndrom {n} <ALGS>med.

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stillbirth, mummification, embryonic death, and infertility syndrome <SMEDI syndrome>

SMEDI-Syndrom {n}VetMed.

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anti-phospholipid (antibody) syndrome <APS, APLA syndrome> [Hughes syndrome]

Antiphospholipidantikörpersyndrom {n} <APS> [auch: Antiphospholipid-Antikörper-Syndrom, Antiphospholipidsyndrom, Antiphospholipid-Syndrom]med.

iliotibial band syndrome <ITBS, ITB syndrome> [runner's knee]

Iliotibialbandsyndrom {n} <ITBS, ITB-Syndrom> [Läuferknie]med.

ilio-tibiales Bandsyndrom {n} <ITBS, ITB-Syndrom> [Läuferknie]med.

gay-related immune deficiency syndrome <GRID syndrome> [obs.] [AIDS]

GRID-Syndrom {n} [veraltet für: AIDS]med.

Osler-Weber-Rendu syndrome <OWR syndrome> [hereditary hemorrhagic telangiectasia]

Osler-Weber-Rendu-Syndrom {n}med.

oligoasthenoteratozoospermia syndrome <OAT syndrome> [also: oligo-astheno-teratozoospermia]

OAT-Syndrom {n}med.

vibration-induced white finger syndrome <VWFS, VWF syndrome>

vibrationsbedingtes vasospastisches Syndrom {n} <VVS>med.

abductor pollicis longus syndrome <APL syndrome> [Peritendinitis crepitans]

Bursitis {f} des Abductor pollicis longus [Intersektionssyndrom]med.

Laurence-Moon-Bardet-Biedl syndrome <LMBBS, LMBB syndrome>

Laurence-Moon-Biedl-Bardet-Syndrom {n} <LMBBS, LMBB-Syndrom>med.

Cauchois-Eppinger-Frugoni syndrome <CEF syndrome> [dated] [portal vein thrombosis]

Cauchois-Eppinger-Frugoni-Syndrom {n} [veraltet] [Pfortaderthrombose]med.

anterior interosseous nerve syndrome [Kiloh-Nevin syndrome] <AINS, AIN syndrome>

Nervus-interosseus-anterior-Syndrom {n}med.

Birt-Hogg-Dube syndrome <BHD syndrome> [also: Birt-Hogg-Dubé syndrome]

Birt-Hogg-Dubé-Syndrom {n} <BHD-Syndrom> [auch: Birt-Hogg-Dube-Syndrom]med.

hand-arm vibration syndrome <HAVS, HAV syndrome>

Hand-Arm-Vibrationssyndrom {n} [vibrationsbedingtes vasospastisches Syndrom]med.

posterior interosseous nerve syndrome <PINS, PIN syndrome>

Nervus-interosseus-posterior-Syndrom {n}med.

multiple congenital ocular anomalies syndrome <MCOA syndrome>

multiples kongenitales okuläres Anomalien-Syndrom {n} [auch: MCOA-Syndrom]VetMed.

keratitis-ichthyosis-deafness syndrome <KID syndrome>

Keratitis-Ichthyosis-Taubheitssyndrom {n}med.

KID-Syndrom {n} [Keratitis-Ichthyosis-Taubheitssyndrom]med.

disseminated intravascular coagulation syndrome <DIC syndrome>

Defibrinationssyndrom {n} [Verbrauchskoagulopathie]med.

DIC-Syndrom {n} [ugs.]med.

• Located on human chromosome 20, the "JAG1" gene is expressed in multiple organ systems in the body and causes the autosomal dominant disorder Alagille syndrome (ALGS) resulting from loss of function mutations within the gene.
• In the case of Alagille syndrome, hepatocyte degeneration is uncommon.
• Alagille syndrome can be extremely difficult to diagnose.
• NOTCH2 is associated with Alagille syndrome and Hajdu–Cheney syndrome.