Blepharo-cheilo-dontic (BCD) syndrome: expanding the phenotype, case report and review of literature.

Farouq K Ababneh, Abdulrahman Al-Swaid, Ahmed Elhag, Talaat Youssef, Saif Alsaif
Author Information
  1. Farouq K Ababneh: Division of Genetics, Department of Pediatrics, King Abdul Aziz Medical City for National Guard, Riyadh, Saudi Arabia.

Abstract

The combination of lagophthalmia, euryblepharon, ectropion of lower eyelids, distichiasis, bilateral cleft lip and palate, and oligodontia comprises the blepharo-cheilo-dontic (BCD) syndrome. This combination has been found sporadically or with positive family history and inherited as an autosomal dominant condition with variable expression. We described a Saudi boy with the cardinal signs consistent with the BCD syndrome. In addition to the common components of BCD syndrome that involve eyelids, lip, and teeth abnormalities, this patient is the third reported BCD case with imperforate anus, the second with thyroid agenesis, and the first with lumbosacral meningomyelocele.

Keywords

MeSH Term

Anus, Imperforate
Cleft Lip
Cleft Palate
Ectropion
Eyelids
Humans
Infant
Infant, Newborn
Infant, Newborn, Diseases
Male
Saudi Arabia
Spinal Dysraphism
Tooth Abnormalities

Word Cloud

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