ISSN: 1308-5727 | E-ISSN: 1308-5735
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Turkish Society for Pediatric Endocrinology and Diabetes
Genoa Syndrome and Central Diabetes Insipidus: A Case Report [J Clin Res Pediatr Endocrinol]
J Clin Res Pediatr Endocrinol. 2010; 2(2): 89-91 | DOI: 10.4274/jcrpe.v2i2.89

Genoa Syndrome and Central Diabetes Insipidus: A Case Report

Bülent Hacıhamdioğlu1, Zeynep Şıklar1, Şenay Savaş Erdeve1, Merih Berberoğlu1, Gülhiz Deda2, Serap Teber Tıraş2, Suat Fitöz3, Gönül Öçal1
1Department Of Pediatric Endocrinology, Ankara University School Of Medicine, Ankara, Turkey
2Department Of Pediatric Neurology, Ankara University School Of Medicine, Ankara, Turkey
3Department Of Radiology, Ankara University School Of Medicine, Ankara, Turkey

Genoa syndrome was first described by Camera et al in 1993 in two patients with semilobar holoprosencephaly (HPE), craniosynostosis and abnormal small hands with cone-shaped epiphyses and hypoplastic terminal phalanges of fingers (OMIM: 601370). In 2001, Lapunzina et al reported a case of craniosynostosis and HPE associated with several other malformations and suggested that these findings could be attributed to a severe form of Genoa syndrome or to a newly recognized syndrome. Endocrinopathies in association with HPE are frequently reported in the literature. Diabetes insipidus, hypothyroidism, hypocortisolism, and growth hormone deficiency are frequently associated with HPE. We here report a case of semilobar HPE, craniosynostosis and cleft lip/palate, possibly a case of Genoa syndrome, associated with central diabetes insipidus.

Keywords: Genoa syndrome,holoprosencephaly,craniosynostosis,cleft lip/palate,central diabetes insipidus

Bülent Hacıhamdioğlu, Zeynep Şıklar, Şenay Savaş Erdeve, Merih Berberoğlu, Gülhiz Deda, Serap Teber Tıraş, Suat Fitöz, Gönül Öçal. Genoa Syndrome and Central Diabetes Insipidus: A Case Report. J Clin Res Pediatr Endocrinol. 2010; 2(2): 89-91
Manuscript Language: English
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