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3-M Syndrome: A Local Case Report
Patient: Male, 3 Final Diagnosis: 3-M syndrome Symptoms: Severe growth retardation • dysmorphic features and skeletal abnormalities Medication: None Clinical Procedure: None Specialty: Pediatric Neurology OBJECTIVE: Rare disease BACKGROUND: 3-M syndrome is an uncommon disease characterized by severe...
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| 發表在: | Am J Case Rep |
|---|---|
| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
International Scientific Literature, Inc.
2019
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6335979/ https://ncbi.nlm.nih.gov/pubmed/30622233 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12659/AJCR.912736 |
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