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March 2021 Vol. 9 No.3
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Merit Research Journal of Medicine and Medical
Sciences (ISSN: 2354-323X) Vol. 9(3) pp.
200-202,
March, 2021
Copyright © 2021 Author(s) retain the copyright
of this article
DOI: 10.5281/zenodo.4627810 |
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Case Report
Bilateral anophthalmia and
clitoris and labia minora agenesis. A case report |
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Viorica Radoi1,2,
Delia Ileana Sabau, Radu Ursu1,2,
Laurentiu Bohiltea1,2,
Oana Toader1,2,
Lucian Pop2 |
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1“Carol Davila” University of Medicine
and Pharmacy, Bucharest, Romania
2“Alessandrescu-Rusescu” National Institute
*Corresponding Author Email: drdeliasabau@hotmail.com
Received: 19 February 2021 I
Accepted: 17 March 2021 I Published: 22 March 2021
I Article ID: MRJMMS-21-024
Copyright © 2021 Author(s) retain the
copyright of this article.
This article is published under the terms of the
Creative Commons Attribution
License 4.0. |
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Abstract |
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Complete bilateral
anophthalmia is the congenital absence of both eyes. Ambiguous
genitalia is the condition in which the patient’s genitalia are
incompletely developed or the baby has characteristics of both
sexes. Pathogenic variants inSOX2 gene are associated with
syndromic microphthalmia, type 3 (OMIM: 206900), with autosomal
dominant inheritance pattern and with AEG syndrome (OMIM
600992). We report the case of a new born baby girl with
bilateral anophthalmia and clitoris and labia minora agenesis,
which originated from in vitro fertilization (IVF). Sequential
genetic testing, QF-PCR, microarray and WES have been performed
and DNA was obtained according to standard procedures. Whole
exome sequencing (WES) identified a mutation in SOX2 (OMIM:
184429) gene, a heterozygous pathogenic variant, NM_003106.4:
c.371dupA p. (Tyr125Valfs*14), highlighting the importance of
this particular gene in embryogenesis, sexualization and the
development of the visual function.It explains the clinical
diagnosis of the patient. We have concluded that this particular
mutation found in the SOX2 gene could be correlated to the
pathological findings, although it was not reported before in
the clinical databases. Furthermore, a prenatal testing
algorithm would be very helpful. Additionally, we want to
highlight the importance of a multidisciplinary team when
diagnosing and managing the follow-up of a fetus with multiple
malformation such as this particular case.
Keywords: Bilateral anophthalmia, Clitoris agenesis,
Labia minora agenesis, SOX2, Syndromic
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