Frontonasal dysplasia Sequence : A case report

Robles‐Bello, María Auxiliadora; Garandawa, Hamman I.; Mustapha, Zainab; Isa, Adiba; Tahir, C; Ngamdu, YB; Machoko, Y; Abubakar, H; Djossi, SK

doi:10.4314/njp.v41i2.17

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“…The parents of an affected child can expect the risk to be 25% for the next child. 7 The embryonic origin of FND is in the period prior to the 28-mm crown-rump length stages. During the 3 rd week of gestation, two areas of thickened ectoderm, the olfactory areas appear immediately under the forebrain in the anterior wall of the stomodeum.…”

Section: Discussionmentioning

confidence: 99%

Frontonasal dysplasia- a rare case report

Sharma¹,

Dogra²,

Malhotra³

et al. 2017

Int J Res Med Sci

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Frontonasal dysplasia (FND) is a rare malformative complex affecting the frontal portion of the face, the eyes and the nose; it may occur singly or associated with other clinical signs. We report here a rare case of a full-term male baby who presented with features of FND. There was no history of consanguinity, no positive family history. Antenatal ultrasonography was normal. Though this baby did not survive because the defects were not compatible for the survival. But the developing nations still have handicap in the management of such cases in term of fiancés, surgical correction of such major defects, education and social support in these patients.

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Section: Discussionmentioning

confidence: 99%