Evidence map›Paper›PMID 41964640›Full record

ArticleThe Journal of clinical endocrinology and metabolism2026

Clinical picture of early-infancy PTH resistance syndromes: is it time to improve diagnostic criteria?

Giulia Del Sindaco, Jugurtha Berkenou, Angela Pagnano, Christelle Audrain, Emanuele Ferrante, Anya Rothenbuhler, Agnès Linglart, Giovanna Mantovani

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Article in The Journal of clinical endocrinology and metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Giulia Del SindacoEndocrinology Unit, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Milan 20122, Italy.ORCID 0000-0002-9050-0150
Jugurtha BerkenouAP-HP, Service d'Endocrinologie et Diabète de l'enfant, Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre 94270, France.
Angela PagnanoEndocrinology Unit, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Milan 20122, Italy.
Christelle AudrainAP-HP, Service d'Endocrinologie et Diabète de l'enfant, Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre 94270, France.
Emanuele FerranteEndocrinology Unit, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Milan 20122, Italy.ORCID 0000-0002-0556-7650
Anya RothenbuhlerAP-HP, Service d'Endocrinologie et Diabète de l'enfant, Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre 94270, France.
Agnès LinglartAP-HP, Service d'Endocrinologie et Diabète de l'enfant, Hôpital Bicêtre Paris-Saclay, Le Kremlin-Bicêtre 94270, France.ORCID 0000-0003-3455-002X
Giovanna MantovaniEndocrinology Unit, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Milan 20122, Italy.ORCID 0000-0002-9065-3886

Funding

ANR IO-COHO-03ESPEFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico DGOS/PNMR3/AP-HPFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico PRIN 2022B5HC29Rare National Disease Plan to the Reference Center
6 · The paper itself

Abstract

contextClinical presentation of inactivating parathyroid hormone (PTH)/PTH-related protein (PTHrP) signaling disorders (iPPSDs, historically pseudohypoparathyroidism [PHP]) exhibits pronounced age-dependence. Indeed, main features, including PTH resistance and brachydactyly (BD), develop during late childhood, while other features (ectopic ossifications, obesity, and hypothyroidism) are most prevalent in toddlers. The latter are included among minor diagnostic criteria; therefore, a substantial diagnostic delay has been reported.

objectiveThe aim of this work is to describe the early natural history of a large cohort of iPPSD/PHP patients to improve diagnosis, with the final goal of proposing new diagnostic criteria for early infancy and reducing diagnostic delay.

methodsWe included 117 patients regularly followed up at 2 European endocrinology tertiary centers, and we retrospectively collected data on the age of onset of main clinical and hormonal features.

resultsIn our cohort the median age at diagnosis was 5.9 years. Age of onset of PTH resistance and BD, major criteria for diagnosis, was significantly different from that of both thyrotropin (TSH) resistance and obesity (median age 6.1, 5.8, 1.85, and 2 years, respectively). Minor diagnostic criteria were more represented than major criteria in children before age 2 years (P = .002). Indeed, in 64% of patients before age 2 years none of the major criteria were observed; conversely, 71% had already developed at least one minor criterion. In particular, 20% had developed TSH resistance and obesity.

conclusionThe clinical picture of iPPSD/PHP in early infancy differs from that of mid-late infancy and adults, thus current diagnostic criteria may not be appropriate for children. We suggest that the combination of early-onset obesity and elevated TSH should raise suspicion and trigger genetic screening before age 2 years.

Indexed as

Parathyroid HormoneParathyroid Hormone-Related ProteinPseudohypoparathyroidismAge of OnsetBrachydactylyChildChild, PreschoolDelayed DiagnosisFemaleHumansInfantMaleRetrospective StudiesParathyroid HormoneParathyroid Hormone-Related Proteindiagnostic criteriainfancynewbornspseudohypoparathyroidism

Identifiers

PMID41964640
PMCPMC13577726

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.