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Fig. 1 | BMC Pediatrics

Fig. 1

From: Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome

Fig. 1

Photographs of the patient showing NS and IP manifestations. a, b front and profile photo respectively pointing facial dysmophism at the age of 1 month with broad forehead, hypertelorism, down-slanting palpebral fissures, a high arched palate, bifid uvula and low set posteriorly rotated ears, long philtrum and epicanthal folds; c-f typical IP manifestations at the age of 1 month showing linear brownish pigmentation involving the trunk and the extremities; g, h front and profile photo of the patient at the age of 1 year highlights the evolution of NS phenotype; i, j evolution of the IP manifestations at the age of 1 year, pectus excatavum becomes more pronounced

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BMC Pediatrics

ISSN: 1471-2431

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