# Orthopedic manifestations and management of nail-patella syndrome: a narrative review

**Authors:** Amandine Beaugé, Viola Sbampato, Oscar Vazquez, Giacomo De Marco, Christina Steiger, Romain Dayer, Dimitri Ceroni

PMC · DOI: 10.3389/fped.2026.1744875 · Frontiers in Pediatrics · 2026-02-04

## TL;DR

Nail-patella syndrome is a rare genetic disorder affecting bones and kidneys, requiring multidisciplinary care and long-term monitoring.

## Contribution

This review provides a comprehensive summary of NPS, focusing on diagnosis, clinical features, and surgical management strategies.

## Key findings

- NPS is caused by LMX1B gene variants and presents with variable skeletal and renal abnormalities.
- Orthopedic management is individualized, with a focus on knee pathology and functional outcomes.
- Early diagnosis and multidisciplinary care are critical to managing complications like nephropathy and glaucoma.

## Abstract

Nail-patella syndrome (NPS) is a rare autosomal dominant disorder characterized by skeletal and renal abnormalities. Diagnosis is primarily clinical, based on four main features: nail dysplasia, patellar and elbow abnormalities, and the presence of iliac horns. NPS affects approximately 1 in 50,000 individuals. Its presentation is highly heterogeneous, even within families, which may delay recognition. Pathogenic variants have been identified in the LMX1B gene located on chromosome 9q34. Although best known for its orthopedic manifestations, NPS may also involve other systems, notably the kidneys and eyes, leading to nephropathy or glaucoma that can progress to severe morbidity. Clinical features may be apparent from birth but will evolve over the life course, thus highlighting the need for long-term monitoring. Management requires a multidisciplinary approach, with orthopedics playing a central role. Surgical decisions, particularly for lower-limb pathology, is individualized and guided by symptom burden and functional impairment. This narrative review summarizes the current literature on NPS, including its epidemiology, etiopathogenesis, clinical manifestations, and natural history. It reviews diagnostic challenges based on clinical and radiologic features. Finally, it critically appraises reported surgical management strategies, with particular emphasis on knee pathology and associated complications, with aims to guide current clinicians.

## Linked entities

- **Genes:** LMX1B (LIM homeobox transcription factor 1 beta) [NCBI Gene 4010]
- **Diseases:** nail-patella syndrome (MONDO:0008061), glaucoma (MONDO:0005041)

## Full-text entities

- **Genes:** LMX1B (LIM homeobox transcription factor 1 beta) [NCBI Gene 4010] {aka FSGS10, LMX1.2, NPS1}, Lmx1b (LIM homeobox transcription factor 1 beta) [NCBI Gene 16917] {aka Icst, LMX1.1, LMX1.2}, ABO (ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase) [NCBI Gene 28] {aka A3GALNT, A3GALT1, GTA, GTB, NAGAT}, NPS (neuropeptide S) [NCBI Gene 594857]
- **Diseases:** tendon injuries (MESH:D013708), nail dysplasia (MESH:C538333), cubital webbing (MESH:C563636), nail deformities (MESH:D009260), intraocular hypertension (MESH:D006973), meniscal anomalies (MESH:D010007), epilepsy (MESH:D004827), Knee involvement (MESH:D007718), Nail abnormalities (MESH:D009264), hypoplastic patella (MESH:D000092462), glenohumeral arthritis (MESH:D001168), scoliosis (MESH:D012600), calcaneovalgus (MESH:D005413), elbow abnormalities (MESH:D000092482), Renal involvement (MESH:C565423), intra-articular abnormality (MESH:D057072), joint abnormalities (MESH:D007592), Knee Injury and Osteoarthritis (MESH:D020370), foot deformities (MESH:D005530), ADHD (MESH:D001289), capitellar hypoplasia of the radial head (MESH:D000092467), synovitis (MESH:D013585), end-stage renal disease (MESH:D007676), neuropsychiatric (MESH:C000631768), ligamentous laxity (MESH:C536012), fetal death (MESH:D005313), lumbar lordosis (MESH:D008141), glaucoma (MESH:D005901), myopathy (MESH:D009135), Shoulder girdle dysplasia (MESH:D020968), ocular hypertension (MESH:D009798), nephropathy (MESH:D007674), skeletal anomalies (MESH:C535534), pelvic anomalies (MESH:D034161), flexion deformities (MESH:D009140), joint instability (MESH:D007593), cubitus valgus deformities (MESH:C564510), elbow deformities (MESH:D000092464), equinus (MESH:D004863), insufficiency fractures (MESH:D015775), dislocation (MESH:D004204), Patellar defects (MESH:D031222), iliac horns (MESH:D017543), dysplasia (MESH:D015792), muscle (MESH:D019042), fractures (MESH:D050723), pain (MESH:D010146), physical (MESH:D059445), normal tension glaucoma (MESH:D057066), muscle hypoplasia (MESH:D009133), complications (MESH:D008107), hypoplasia (MESH:D000080344), atrophy (MESH:D001284), valgum deformities (MESH:D056304), pre-eclampsia (MESH:D011225), neurological involvement (MESH:C538190), weakness (MESH:D018908), patellar tendon rupture (MESH:D012421), psychiatric (MESH:D001523), aplasia (MESH:C536482)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** Q65P, 194 A>C

## Full text

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## References

78 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913535/full.md

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Source: https://tomesphere.com/paper/PMC12913535