# Hypopituitarism and Other Endocrinopathies as a Consequence of Septo-Optic Dysplasia

**Authors:** Anjana Swami, Monish Sharma, Lindsey VanDyke

PMC · DOI: 10.7759/cureus.82329 · Cureus · 2025-04-15

## TL;DR

This paper presents a case of a woman with septo-optic dysplasia and related endocrine issues, highlighting the long-term management and positive outlook.

## Contribution

The novelty lies in the detailed case report of a rare disorder with multiple endocrinopathies and successful hormone treatment.

## Key findings

- The patient was diagnosed with SOD after years of investigation.
- She developed multiple endocrine pathologies linked to her SOD.
- Hormone therapy is effectively managing her conditions with a favorable prognosis.

## Abstract

Septo-optic dysplasia (SOD) is a rare disorder that affects early brain development. It is characterized and diagnosed by the presence of at least two out of the following: optic nerve hypoplasia, agenesis of the septum pellucidum, and pituitary hypoplasia. Currently, the cause of the disease is largely thought to be sporadic and involves both genetic and environmental factors. We report the case of a 29-year-old female patient who was diagnosed with SOD after years of diagnostic investigation as well as the emergence of multiple endocrine pathologies related to her SOD. The patient is currently being treated with a variety of hormones to manage her endocrinopathies and is predicted to have a favorable prognosis.

## Linked entities

- **Diseases:** septo-optic dysplasia (MONDO:0008428), hypopituitarism (MONDO:0005152)

## Full-text entities

- **Diseases:** agenesis of the septum pellucidum (MESH:C535562), SOD (MESH:D025962), optic nerve hypoplasia (MESH:D000080344), Hypopituitarism (MESH:D007018), endocrine pathologies (MESH:D004700), pituitary hypoplasia (MESH:D010900), Endocrinopathies (MESH:C567425)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12084846/full.md

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Source: https://tomesphere.com/paper/PMC12084846