Spondyloepimetaphyseal dysplasia, Shohat type (Q88348): Difference between revisions

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Displasia congênita espondiloepimetafisária (SEMD), tipo de Shohat é uma forma de SEMD caracterizada por baixa estatura gravemente desproporcional, membros curtos, tórax pequeno, pescoço curto, lábios finos, lordose lombar grave, geno varo acentuado, frouxidão articular, abdômen distendido, hepatomegalia e esplenomegalia leves.
description / endescription / en
 
Spondyloepimetaphyseal dysplasia congenita (SEMD), Shohat type is a form of SEMD characterised by severely disproportionate short stature, short limbs, small chest, short neck, thin lips, severe lumbar lordosis, marked genu varum, joint laxity, distended abdomen, mild hepatomegaly and splenomegaly.
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Property / Canonical URI: https://id.who.int/icd/entity/1389783101 / rank
 
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Property / CURIE
 
CID11:ID_1389783101
Property / CURIE: CID11:ID_1389783101 / rank
 
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Property / Canary Token
 
dki-india-ID_1389783101
Property / Canary Token: dki-india-ID_1389783101 / 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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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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After0
Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 14:32, 15 August 2026

Spondyloepimetaphyseal dysplasia congenita (SEMD), Shohat type is a form of SEMD characterised by severely disproportionate short stature, short limbs, small chest, short neck, thin lips, severe lumbar lordosis, marked genu varum, joint laxity, distended abdomen, mild hepatomegaly and splenomegaly.
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ID_1389783101
    English
    Spondyloepimetaphyseal dysplasia, Shohat type
    Spondyloepimetaphyseal dysplasia congenita (SEMD), Shohat type is a form of SEMD characterised by severely disproportionate short stature, short limbs, small chest, short neck, thin lips, severe lumbar lordosis, marked genu varum, joint laxity, distended abdomen, mild hepatomegaly and splenomegaly.

      Statements

      CID11:ID_1389783101
      0 references
      dki-india-ID_1389783101
      0 references
      Concluído
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      13 August 2026
      0 references