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Le syndrome de Goltz est une dysplasie congénitale des tissus dérivés du mésoectoderme transmis sur le mode de l’hérédité dominante liée à l’X par mutations du gène PORCNsitué en Xp11.23. Les lésions cutanées, réparties en plages, peuvent être associées à diverses malformations congénitales. Nous rapportons un cas de syndrome de Goltz chez 1 nouveau-né de sexe féminin de race noire. Les lésions cutanéophanériennes...
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