Pyknoachondrogenesis (Q106920): Difference between revisions

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A picnoacondrogênese é uma osteocondrodisplasia letal caracterizada pela presença de osteosclerose grave generalizada, encurtamento extremo dos membros e hidropsia fetal pré-natais, ou por macrocefalia, edema palpebral, achatamento nasal, baixa implantação das orelhas, pescoço curto, um tronco curto e largo, o abdome proeminente e nanismo micromélico grave ao nascimento.
description / endescription / en
 
Pyknoachondrogenesis is a lethal skeletal osteochondrodysplasia characterised by severe generalised osteosclerosis with extreme shortening of the limbs and hydrops fetalis prenatally, or a large head, palpebral oedema, a flat nose, low-set ears, a short neck, a short and wide trunk, a prominent abdomen, and severe micromelic dwarfism at birth.
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Property / Canonical URI: https://id.who.int/icd/entity/588435239 / rank
 
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CID11:ID_588435239
Property / CURIE: CID11:ID_588435239 / rank
 
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dki-india-ID_588435239
Property / Canary Token: dki-india-ID_588435239 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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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
Before0
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Property / Collection date: 16 August 2026 / rank
 
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Latest revision as of 13:55, 17 August 2026

Pyknoachondrogenesis is a lethal skeletal osteochondrodysplasia characterised by severe generalised osteosclerosis with extreme shortening of the limbs and hydrops fetalis prenatally, or a large head, palpebral oedema, a flat nose, low-set ears, a short neck, a short and wide trunk, a prominent abdomen, and severe micromelic dwarfism at birth.
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ID_588435239
    English
    Pyknoachondrogenesis
    Pyknoachondrogenesis is a lethal skeletal osteochondrodysplasia characterised by severe generalised osteosclerosis with extreme shortening of the limbs and hydrops fetalis prenatally, or a large head, palpebral oedema, a flat nose, low-set ears, a short neck, a short and wide trunk, a prominent abdomen, and severe micromelic dwarfism at birth.

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      CID11:ID_588435239
      0 references
      dki-india-ID_588435239
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      Concluído
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      16 August 2026
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