# Severe growth faltering and persistent hyperchloremic metabolic acidosis as early clues of renal tubular acidosis in a neonate: a case report

**Authors:** Nafisa Mariam, Monira Sarmin, Nusrat Jahan Shaly, Mosharrat Tabassum, Shamima Sharmin Shikha, Didarul Haque Jeorge, Farzana Afroze, Lubaba Shahrin, Tahmeed Ahmed, Chowdhury Ali Kawser, Mohammod Jobayer Chisti

PMC · DOI: 10.1093/omcr/omaf294 · Oxford Medical Case Reports · 2026-02-18

## TL;DR

A neonate with severe growth issues and acidosis was diagnosed with renal tubular acidosis, highlighting the importance of early detection in resource-limited settings.

## Contribution

This case report highlights the early signs of renal tubular acidosis in neonates in resource-limited settings.

## Key findings

- A neonate presented with growth faltering and metabolic acidosis, leading to a diagnosis of proximal renal tubular acidosis.
- Persistent hyperchloremic acidosis despite diarrhoea and septic shock indicated underlying renal dysfunction.
- Early diagnosis and treatment are crucial to prevent complications like electrolyte disorders and bony deformities.

## Abstract

Renal tubular acidosis (RTA) often presents as failure to thrive in children. In a resource-limited country, the diagnosis of renal tubular acidosis can be delayed or even missed because of the co-existing high burden of malnutrition. Here we report a case of a neonate/infant who presented with diarrhoea and failure to thrive and subsequently developed septic shock. During the management of the child, proximal renal tubular acidosis was diagnosed based on the persistence of metabolic acidosis with hyperchloremia. Proximal renal tubular acidosis (pRTA) can lead to complications, such as electrolyte disorders, bony deformities. Prompt diagnosis, appropriate treatment, and long-term follow-up are imperative for achieving good outcomes.

## Linked entities

- **Diseases:** renal tubular acidosis (MONDO:0001909), proximal renal tubular acidosis (MONDO:0008369)

## Full-text entities

- **Genes:** SLC4A4 (solute carrier family 4 member 4) [NCBI Gene 8671] {aka HNBC1, KNBC, NBC1, NBC2, NBCe1, NBCe1-A}
- **Diseases:** failure to thrive (MESH:D005183), pulmonary tuberculosis (MESH:D014397), Type 3 RTA (MESH:C537759), infections (MESH:D007239), sclerema (MESH:D012593), acidosis (MESH:D000138), herpes simplex (MESH:D006561), bone deformities (MESH:D001847), dehydrating diarrheas (MESH:D003681), renal stones (MESH:D007669), polydipsia (MESH:D059606), cough (MESH:D003371), rubella (MESH:D012409), urinary infections (MESH:D014552), Proximal renal tubular acidosis (MESH:D000141), weight loss (MESH:D015431), TORCH infection (MESH:C535607), Malnourished (MESH:D044342), band keratopathy (MESH:C562399), HIV (MESH:D015658), septic shock (MESH:D012772), sepsis (MESH:D018805), rickets (MESH:D012279), bony deformities (MESH:D018213), toxoplasmosis (MESH:D014123), watery diarrhoea (MESH:D003969), cataract (MESH:D002386), constipation (MESH:D003248), hypokalemia (MESH:D007008), glaucoma (MESH:D005901), muscle weakness (MESH:D018908), Failure to (MESH:D051437), anorexia (MESH:D000855), electrolyte disorder (MESH:D014883), Polyuria (MESH:D011141), shock (MESH:D012769), Diarrhoeal Disease (MESH:D004194), autosomal recessive condition (MESH:D020763), Fanconi syndrome (MESH:D005198), growth faltering (MESH:D006130), fever (MESH:D005334), genetic defect (MESH:D030342), vomiting (MESH:D014839), blindness (MESH:D001766), acute malnutrition (MESH:D000067011), cholera (MESH:D002771), cytomegalovirus (MESH:D003586), weight gain (MESH:D015430), diarrhea (MESH:D003967), acute kidney injury (MESH:D058186), proximal (MESH:D014897), pneumonia (MESH:D011014), wasting (MESH:D019282)
- **Chemicals:** HCO3- (MESH:D001639), Amikacin (MESH:D000583), Monira Sarmin (-), potassium (MESH:D011188), hydrogen (MESH:D006859), dopamine (MESH:D004298), calcium (MESH:D002118), creatinine (MESH:D003404), glucose (MESH:D005947), Ampicillin (MESH:D000667), ammonium chloride (MESH:D000643), uric acid (MESH:D014527), adrenaline (MESH:D004837), vitamin D (MESH:D014807), phosphorus (MESH:D010758), Gentamicin (MESH:D005839), water (MESH:D014867), Ceftazidime (MESH:D002442)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12915056/full.md

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Source: https://tomesphere.com/paper/PMC12915056