# Differential Pregnancy Decisions in a Woman With a Recurrent Prenatal Diagnosis of Hypophosphatasia

**Authors:** Taiyo Oguro, Ryuhei Nagai, Yuta Shimomoto

PMC · DOI: 10.7759/cureus.87005 · Cureus · 2025-06-29

## TL;DR

A woman's decisions about two pregnancies with hypophosphatasia (HPP) were influenced by the timing and quality of medical counseling.

## Contribution

The study emphasizes the importance of early, balanced, and multidisciplinary counseling for rare prenatal conditions like HPP.

## Key findings

- Late counseling led to termination, while early multidisciplinary counseling led to continuation of pregnancy.
- Prenatal benign HPP can have a favorable prognosis when managed with informed decision-making.
- Specialists often lack experience with rare diseases like HPP, affecting counseling outcomes.

## Abstract

Hypophosphatasia (HPP) is a rare inherited bone disorder caused by ALPL gene mutations, leading to reduced alkaline phosphatase (ALP) activity and impaired bone mineralization. Although its prevalence is relatively higher in Japan, prenatal diagnosis remains challenging. In particular, obstetricians and clinical geneticists, who are typically involved in prenatal assessment, often have limited experience with this condition due to its rarity. Among the various types of HPP, the prenatal benign form has a favorable prognosis, yet awareness and understanding of this specific subtype are limited.

We report a case involving two separate pregnancies in the same woman, both diagnosed prenatally with HPP. During the second pregnancy, counseling was provided at 21 weeks by a physician. Given the rarity of HPP, even specialists such as obstetricians, pediatricians, or clinical geneticists often have limited direct clinical experience with the condition. Consequently, the counseling leaned toward a negative outlook, and the patient opted for termination. In contrast, during the third pregnancy, counseling began at nine weeks with detailed and balanced information, informed by the previous case and supported by a multidisciplinary team. This time, the patient elected to continue the pregnancy. The neonate was diagnosed with prenatal benign HPP and showed favorable clinical progress.

This case highlights how the timing, quality, and balance of prenatal counseling can significantly influence parental decision-making in pregnancies complicated by rare diseases. In cases of rare conditions such as HPP, early and accurate counseling by an experienced multidisciplinary team is essential to support informed and autonomous decisions.

## Linked entities

- **Genes:** ALPL (alkaline phosphatase, biomineralization associated) [NCBI Gene 249]
- **Proteins:** ALPP (alkaline phosphatase, placental)
- **Diseases:** Hypophosphatasia (MONDO:0018570), HPP (MONDO:0009948)

## Full-text entities

- **Genes:** ALPL (alkaline phosphatase, biomineralization associated) [NCBI Gene 249] {aka AP-TNAP, APTNAP, HOPS, HPPA, HPPC, HPPI}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}
- **Diseases:** impaired bone mineralization (MESH:D012080), inherited bone disorder (MESH:D000080984), HPP (MESH:D007014)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC12212621/full.md

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Source: https://tomesphere.com/paper/PMC12212621