October 3, 2025Case Reports in PediatricsOpen Access

Prolidase Deficiency Presenting With Pulmonary Arteriovenous Malformations and Seizures: Report of Two Cases From Iran

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Authors

APAli PajouhiLorestan University of Medical Sciences RRRouhollah RohaniTehran University of Medical Sciences VZVahid ZiaeeUniversity of Tehran

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Implication

Case reports illustrate complex symptoms of prolidase deficiency in individuals from Iran, suggesting broader diagnosis criteria and management strategies.

Key Points

Prolidase deficiency presents with diverse symptoms, including pulmonary arteriovenous malformations and seizures, complicating diagnosis.
Case details highlight two distinct presentations of prolidase deficiency, with a 17-year-old male and a one-year-old female showing atypical symptoms.
The absence of standard diagnostic methods for prolidase deficiency indicates the need for enhanced awareness and protocols.
Future studies should consider different ethnic and geographical groups to improve understanding of prolidase deficiency and its manifestations.

Cite This Study

Pajouhi et al. (2025) studied this question.

synapsesocial.com/papers/68e02f40f0e39f13e7fa2ac5 https://doi.org/10.1155/crpe/9929135

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Implication

Case reports illustrate complex symptoms of prolidase deficiency in individuals from Iran, suggesting broader diagnosis criteria and management strategies.

Prolidase Deficiency Presenting With Pulmonary Arteriovenous Malformations and Seizures: Report of Two Cases From Iran

Discussion

Member takes

Implication

Key Points

Cite This Study

Prolidase Deficiency Presenting With Pulmonary Arteriovenous Malformations and Seizures: Report of Two Cases From Iran

Discussion

Member takes

Implication

Key Points

Cite This Study

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