A Rare Case of Complete Cryptophthalmos and Suspected Fraser’s Syndrome in a Female Neonate

Author:

Ramadugu Rithika1,Kuppili Satwik2,Suvvari Tarun Kumar34,Lella Vindhya Vasini2ORCID,Thomas Vimal5

Affiliation:

1. Kamineni Academy of Medical Sciences and Research Centre, Hyderabad, Telangana, India

2. Konaseema Institute of Medical Sciences (KIMS), Amalapuram, Andhra Pradesh, India

3. Rangaraya Medical College, Kakinada, Andhra Pradesh, India

4. Squad Medicine and Research (SMR), Andhra Pradesh, India

5. Tbilisi State Medical University, Tbilisi, Georgia

Abstract

Cryptophthalmos is a rare congenital eye anomaly characterized by the absence of the palpebral fissure. Cryptophthalmos is often associated with Fraser’s syndrome. We present a case of 3 days old female Asian neonate with complete unilateral cryptophthalmos, with the absence of a right eyelid. On inspection, there is an absence of eyelid, eyebrow and eyelashes in the right eye, collectively known as adnexal structures. The left eye was apparently normal. As per the parent’s decision, surgical intervention was not pursued due to the poor visual prognosis. We advised prenatal genetic screening and testing for future pregnancies. These findings suggest the importance of genetic counseling and testing in cases of cryptophthalmos to identify potential genetic mutations and facilitate appropriate management.

Publisher

SAGE Publications

Subject

General Medicine

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