Peer Reviewed

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Van der Woude Syndrome

Volume 60 - Issue 5 - May 2020

AUTHORS:
Brina Bui, BA • Makenna Arca, BS • Lynnette J. Mazur, MD, MPH

AFFILIATION:
McGovern Medical School at UT Health, Houston, Texas

CITATION:
Bui B, Arca M, Mazur LJ. Van der Woude syndrome. Consultant. 2020;60(5):e11. doi:10.25270/con.2020.03.00020

Received November 19, 2019. Accepted February 28, 2020.

DISCLOSURE:
The authors report no relevant financial relationships.

CORRESPONDENCE:
Lynnette J. Mazur, MD, MPH, McGovern Medical School at UT Health, 6431 Fannin St, Houston, TX 77030 (lynnette.j.mazur@uth.tmc.edu)

On a medical mission to treat the indigenous Cabécar people of Costa Rica, a 4-year-old girl and her 15-year-old brother came to the pediatric clinic for a checkup. On physical examination, the girl had a well-healed cleft lip scar and lower lip pits, and her brother had lower lip pits with no other abnormalities. The children’s mother exhibited less-obvious lower lip pits (Figures 1-3).

Fig 1
Figure 1. A 4-year-old girl with well-healed cleft lip scar and lower lip pits.

Fig 2
Figure 2. A 15-year-old boy, the girl’s brother, with lower lip pits.

Fig 3
Figure 3. The children’s mother with less-obvious lower lip pits.

DISCUSSION

Van der Woude syndrome (VWS), first described in 1845, manifests clinically as lower lip pits and cleft lip and/or palate.1 It occurs in an estimated 3.6 per 100,000 live births, and it exhibits an autosomal dominant inheritance pattern with an estimated penetrance of 89% to 99% and variable expressivity.2,3

Approximately 70% of VWS cases are associated with deletions or mutations of the interferon regulatory factor 6 gene (IRF6) at 1q32-q41.4-7 Mutations in the grainyhead-like transcription factor 3 gene (GRHL3) have been identified in several families with VWS, providing evidence for locus heterogeneity.8

VWS is the most common cause of syndromic clefts and syndromic lip pits, accounting for 2% and 80%, respectively.7,9,10 Lower lip pits are the most common manifestation of VWS, and the lip pits range from subtle depressions to bilateral fistulae with or without drainage of minor salivary glands.1 VWS can also present with hypodontia, hypoplasia, ankyloglossia, high arched palate, limb anomalies, congenital heart defects, finger syndactyly, syngnathia, and ankyloblepharon.11,12

The differential diagnosis (Table) includes popliteal pterygium syndrome (PPS), commissural and upper lip pits, clefts without pits due to variable expressivity, aganglionic megacolon with lip pits and cleft palate, and type 1 orofacial digital syndrome.13 VWS and PPS are similar in that both can present with lower lip pits with cleft lip and/or palate. However, patients with PPS may also have bilateral popliteal webs, genital and nail anomalies, and oral synechiae. It is hypothesized that PPS and VWS are allelic variants of the same condition.14 Therefore, individuals with VWS can have children with PPS.

Table

For children who present with signs and symptoms of VWS, a thorough orofacial examination must be performed to identify the type and extent of pitting and/or clefting. These patients may also have cardiovascular defects, so a thorough physical examination is also important. It is best to approach these patients with a multidisciplinary team including dentists, otolaryngologists, pediatric plastic surgeons, geneticists, genetic counselors, social workers, and occupational, speech, and physical therapists.

Pediatric plastic surgeons correct the cleft lip and/or cleft palate using the same approach as is used for nonsyndromic cleft lip and/or cleft palate. Lip pits can be removed during a minor surgical procedure in which saliva drainage is rerouted and lip aesthetics are improved. A pediatric geneticist is helpful in explaining the 50% risk of occurrence in the children of a patient with VWS.

REFERENCES:

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