Craniomicromelic syndrome (Q93981): Difference between revisions

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A síndrome craniomicromélica é um distúrbio esquelético muito raro, caracterizado por retardo do crescimento intrauterino, sob ossificação do crânio com fontanelas grandes, membros curtos com falanges ausentes e sindactilia dos dedos das mãos e pés. As características dismórficas incluem face estreita com pequenas fissuras palpebrais, nariz pontiagudo, microstomia, micrognatia e orelhas de implantação baixa e giradas posteriormente.
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Craniomicromelic syndrome is a very rare skeletal disorder characterised by intrauterine growth retardation, under ossification of the skull with large fontanels, short limbs with absent phalanges and finger and toe syndactyly. Dysmorphic features include narrow face with small palpebral fissures, small pointed nose, microstomia, micrognathia and low-set and posteriorly rotated ears.

Revision as of 09:05, 16 August 2026

Craniomicromelic syndrome is a very rare skeletal disorder characterised by intrauterine growth retardation, under ossification of the skull with large fontanels, short limbs with absent phalanges and finger and toe syndactyly. Dysmorphic features include narrow face with small palpebral fissures, small pointed nose, microstomia, micrognathia and low-set and posteriorly rotated ears.
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ID_1734157428
    English
    Craniomicromelic syndrome
    Craniomicromelic syndrome is a very rare skeletal disorder characterised by intrauterine growth retardation, under ossification of the skull with large fontanels, short limbs with absent phalanges and finger and toe syndactyly. Dysmorphic features include narrow face with small palpebral fissures, small pointed nose, microstomia, micrognathia and low-set and posteriorly rotated ears.

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