Wordt geladen...
Laurence-Moon-Bardet-Biedl Syndrome: A Case Report
Laurence-Moon-Bardet-Biedl syndrome (LMBBS), a rare autosomal recessive defect, mostly occurs in children born from consanguineous marriages. The major features of this syndrome are cone-rod dystrophy, polydactyly, obesity, learning disabilities, hypogonadism in males, renal anomalies, nystagmus, sp...
Bewaard in:
| Gepubliceerd in: | Cureus |
|---|---|
| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Cureus
2019
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6820889/ https://ncbi.nlm.nih.gov/pubmed/31696011 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.5618 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|