Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmen-tation changes and minor facial malformations. It has four clinical variants. We report the case of a girl who, like her mother, was affected by this syndrome. The diagnosis was made after detection and treatment of deafness

Cestari, Tania Ferreira

Escobar, Gabriela Fortes

Nazar, Fernanda Luca

Peruzzo, Juliano

Tubone, Mariana Quirino

Anais Brasileiros de Dermatologia

English

Lume 5.8

SYNDROME IN QUESTION*Juliano Peruzzo1 Fernanda Luca Nazar1Mariana Quirino Tubone2 Gabriela Fortes Escobar1Tania Ferreira Cestari1 ▲ Received on 25.12.2013.Approved by the Advisory Board and accepted for publication on 10.02.2014.*  Study conducted at the Hospital de Clínicas de Porto Alegre - Federal University of Rio Grande do Sul (UFRGS) – Porto Alegre (RS), Brazil.  Financial Support: None. Confl ict of Interest: None.1 Federal University of Rio Grande do Sul (UFRGS) – Porto Alegre (RS), Brazil. 2   Private Clinic– Porto Alegre (RS), Brazil.  ©2015 by Anais Brasileiros de DermatologiaDOI: http://dx.doi.org/10.1590/abd1806-4841.20153343 Abstract: Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmen-tation changes and minor facial malformations. It has four clinical variants. We report the case of a girl who, like her mother, was affected by this syndrome. The diagnosis was made after detection and treatment of deafness.Keywords: Skin diseases, genetic; Genetic diseases, inborn; Deafness; Waardenburg syndrome.589 CASE REPORTA 12-year-old girl sought dermatological consultation regarding warts. She had a history of bilateral sensorineural deafness, fi rst noticed at the age of 2 years, and received cochlear implant in right ear at the age of 5 years.Physical examination revealed perioral warts. In addition, we noticed isohypochromia iridis, dystopia canthorum, hypertrichosis of the medial part of the eyebrows (synophrys), slight obliteration of the philtrum, and achromic patches on the back of the fi ngers of the right hand (Figure 1). We noted that the girl’s mother had heterochromia of the left eye and achromic patches on the anterior aspect of the left forearm (Figure 2). Moreover, the mother reported early graying of her hair and that the patient’s sister also had similar patches.An ophthalmologic evaluation revealed diffuse thinning of the retinal pigment epithelium. An Bras Dermatol. 2015;90(4):589-90.FIGURE 1: A. Isohy-pochromia iridum, canthorum dystopia, broad nasal bridge, hypertrichosis of the medial part of the eyebrows and obliteration of the philtrum. We can also see perioral keratotic papules compatible with viral warts. B. Achromic maculae and patches on the medial phalanges of the fi ngers of the right handABFIGURE 2: Isohy-pochromia iridum in the patient (left) and heterochromia iridum in the pa-tient’s mother (right). We can see oblitera-tion of the philtrum and a broad nasal rootRevistaABD4Vol90ingles.indd   589 12/08/15   10:32590 Peruzzo J, Nazar FL, Tubone MQ, Escobar GF, Cestari TFDISCUSSIONWaardenburg syndrome (WS) is an inherited disease with an estimated incidence of 1: 42,000 births. 1,2 It has 4 clinical variants, which share varying degrees of sensorineural hearing loss and changes in pigmentation.In most cases, it is an autosomal dominant disorder caused by mutations in the PAX3 gene on chromosome 2q. These mutations result in changes in the differentiation, survival and migration of melanocytes derived from the neural crest in the embryonic period. 3-5 The great clinical variability of the syndrome is attributed to different penetrance and expression of the responsible genes. 6SW type 1 is the classical form. 2 It is characterized by varying degrees of hearing loss, defects in neural crest-derived structures and changes in pigmentation. 7Deafness, which is of sensorineural origin, may be unilateral or bilateral, total or partial. It occurs in approximately 20% of patients. 7 About 2% of all cases of congenital deafness are due to the SW. 1.4Dystopia canthorum (or telecanthus) is characterized by an increased distance between the inner corner of the eyelids, with normal distance between the pupils. It is a minor defect, the most common fi nding in SW type 1 (98% of cases) and the main feature that distinguishes it from other types of SW. 4,8,9 Other manifestations include broad nasal root, obliteration of the philtrum, synophrys (confl uence of the eyebrows) and low anterior hairline.3The main pigmentary changes of SW type 1 are heterochromia or isohypocromia iridum, poliosis and early whitening of the hair. In addition, there may be retinal pigmentary changes, areas of leukoderma and hyperchromic maculae.Diagnosis is based on clinical fi ndings (Chart 1). For diagnosis, 2 major criteria or 1 major criterium and 2 minor criteria must be present. 2.9There is no specifi c treatment for this syndrome. Early diagnosis enables the treatment of deafness. Dermatological fi ndings are often unnoticed. However, they are essential for early diagnosis. Other than allowing the treatment of deafness, early diagnosis prevents permanent disabilities and is thus important for the development of the child.The patient in our case had 4 major criteria and one minor criterium, which confi rmed the diagnosis of SW type 1. Furthermore, the patient had received cochlear implant at an early age and showed improvement of hearing loss. ❑ An Bras Dermatol. 2015;90(4):589-90.How to cite this article: Peruzzo J, Nazar FL, Tubone MQ, Escobar GF, Cestari TF. Waardenburg syndrome type 1. An Bras Dermatol. 2015;90(4):589-90.REFERENCES1. Konno P, Silm H. Waardenburgsyndrome. J EurAcadDermatolVenereol. 2001;15:330-3.2. Omar ED, Oliveira ZNP, Machado-Rivitti MC. Do youknowthissyndrome? Waardenburgsyndrometype 2B. AnBrasDermatol. 2007;82:186-9.3. Dourmishev AL, Dourmishev LA, Schwartz RA, Janniger CK. Waardenburg syndrome. Int J Dermatol. 1999;38:656-63.4. Nayak CS, Isaacson G.World wide distribution of Waardenburg syndrome. Ann OtolRhinolLaryngol. 2003;112:817-20.5. Nasser LS, Paranaíba LMR, Frota AC, Gomes A, Versiani G, Júnior HM. Síndrome de Waardenburg - aspectos oftalmológicos e critérios de diagnóstico: relatos de casos. Arq Bras Oftalmol. 2012;75:352-5.6. Demirci GT, Atıs G, Altunay IK. Waardenburgsyndrometype1: a case report. Dermatol Online J. 2011;17:3.7. Kumar S, Rao K. Waardenburgsyndrome: a raregeneticdisorder, reportoftwo cases. Indian J Hum Genet. 2012;18:254-5.8. Goenaga AM, Ferreira LC, Ferreira RC, Cestari TF. Síndrome de Waardenburg: relato de dois casos e revisão da literatura. An Bras Dermatol. 1996;71:419-23.9. Eigelshoven S, Kameda G, Kortüm AK, Hübsch S, Angerstein W, Singh P,et al. Waardenburg syndrome type I with heterochromia iridis and circumscribed hypopigmentation of the skin. Pediatr Dermatol. 2009;26:759-61.  MAILING  ADDRESS:Juliano PeruzzoRua Ramiro Barcelos, 2350Bairro Santa Cecília90035-903. Porto Alegre, RS, Brazil.E-mail:julianoperuzzo@gmail.comCHART 1: Diagnostic criteria for Waardenburg syndrome type 1MAJOR CRITERIA MINOR CRITERIAHair hypopigmentation Congenital leukodermaPigmentary change of the iris Early graying of the hairDystopia canthorum SynophrysSensorineural hearing loss Broad nasal rootFirst-degree relative with WS Hypoplasia of the  nasal alaRevistaABD4Vol90ingles.indd   590 19/08/15   15:13

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