Draft:PARC syndrome: Difference between revisions
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{{short description|Congenital disorder}} |
{{short description|Congenital disorder}} |
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{{Infobox medical condition |
{{Infobox medical condition |
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| name = PARC syndrome |
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| specialty = {{hlist | [[Medical genetics]] | [[pediatrics]]}} |
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| symptoms = {{hlist | [[Alopecia]] | [[atrophy]] | [[cleft palate]] | [[hyperpigmentation]] | [[hypopigmentation]] | [[overbite]] | [[spider veins]]}} |
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'''PARC syndrome'''{{efn|Poikiloderma, alopecia, retrognathism, and cleft palate<ref>{{Cite journal |last=Verloes |first=A. |last2=Soyeur-Broux |first2=M. |last3=Arrese-Estrada |first3=J. |last4=Piérard-Franchimont |first4=C. |last5=Dodinval |first5=P. |last6=Piérard |first6=G. E. |date=1990 |title=Poikiloderma, alopecia, retrognathism and cleft palate: the PARC syndrome. Is this an undescribed dominantly inherited syndrome? |url=https://pubmed.ncbi.nlm.nih.gov/2242783/ |journal=Dermatologica |volume=181 |issue=2 |pages=142–144 |doi=10.1159/000247904 |issn=0011-9075 |pmid=2242783}}</ref>}} is a rare |
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== Signs and symptoms == |
== Signs and symptoms == |
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== Research == |
== Research == |
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== Notes == |
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{{notelist}} |
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== References == |
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{{Reflist}} |
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Latest revision as of 13:52, 13 June 2024
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PARC syndrome[a] is a rare
Signs and symptoms
[edit]Causes
[edit]Diagnosis
[edit]Prognosis
[edit]Epidemiology
[edit]Research
[edit]Notes
[edit]References
[edit]- ^ Verloes, A.; Soyeur-Broux, M.; Arrese-Estrada, J.; Piérard-Franchimont, C.; Dodinval, P.; Piérard, G. E. (1990). "Poikiloderma, alopecia, retrognathism and cleft palate: the PARC syndrome. Is this an undescribed dominantly inherited syndrome?". Dermatologica. 181 (2): 142–144. doi:10.1159/000247904. ISSN 0011-9075. PMID 2242783.