Distal arthrogryposis type 3 (Q104860): Difference between revisions

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A artrogripose distal tipo 3 (também conhecida como Síndrome de Gordon) é uma doença genética extremamente rara que se caracteriza pela combinação de camptodactilia (uma fixação permanente de vários dedos em uma posição flexionada), pé torto ou talipes (flexão anormal do pé para dentro) e, em 25% dos pacientes, fenda palatina. A inteligência é normal, mas, em alguns casos, anormalidades adicionais (por exemplo, escoliose e criptorquidia) também podem estar presentes.
description / endescription / en
 
Distal arthrogryposis type 3 (aka Gordon Syndrome) is an extremely rare genetic disorder that is characterised by the combination of camptodactyly (a permanent fixation of several fingers in a flexed position), clubfoot or talipes (abnormal bending inward of the foot), and, in 25 % of patients, cleft palate. Intelligence is normal but in some cases, additional abnormalities (for example, scoliosis and cryptorchidism) may also be present.
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Property / Canonical URI: https://id.who.int/icd/entity/1444357813 / rank
 
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CID11:ID_1444357813
Property / CURIE: CID11:ID_1444357813 / rank
 
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dki-india-ID_1444357813
Property / Canary Token: dki-india-ID_1444357813 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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16 August 2026
Timestamp+2026-08-16T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 16 August 2026 / rank
 
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Latest revision as of 10:43, 17 August 2026

Distal arthrogryposis type 3 (aka Gordon Syndrome) is an extremely rare genetic disorder that is characterised by the combination of camptodactyly (a permanent fixation of several fingers in a flexed position), clubfoot or talipes (abnormal bending inward of the foot), and, in 25 % of patients, cleft palate. Intelligence is normal but in some cases, additional abnormalities (for example, scoliosis and cryptorchidism) may also be present.
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ID_1444357813
    English
    Distal arthrogryposis type 3
    Distal arthrogryposis type 3 (aka Gordon Syndrome) is an extremely rare genetic disorder that is characterised by the combination of camptodactyly (a permanent fixation of several fingers in a flexed position), clubfoot or talipes (abnormal bending inward of the foot), and, in 25 % of patients, cleft palate. Intelligence is normal but in some cases, additional abnormalities (for example, scoliosis and cryptorchidism) may also be present.

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      CID11:ID_1444357813
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      dki-india-ID_1444357813
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      Concluído
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      16 August 2026
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