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{{short description|Congenital disorder}}
{{Infobox medical condition
| name = PARC syndrome
| specialty = {{hlist | [[Medical genetics]] | [[pediatrics]]}}
| symptoms = {{hlist | [[Alopecia]] | [[atrophy]] | [[cleft palate]] | [[hyperpigmentation]] | [[hypopigmentation]] | [[overbite]] | [[spider veins]]}}
}}
'''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
== Signs and symptoms ==
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== Research ==
== Notes ==
{{notelist}}
== References ==
{{Reflist}}
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