Evidence map›Paper›PMID 42823987›Full record

ReviewFrontiers in endocrinology2026

Consensus statement on the management of Achondroplasia in the Middle East.

Nandu Thalange, Tawfeg Ben Omran, Afaf Alsagheir, Khalid Hussain, Maha Faden, Mona Aglan, Sareea Alremeithi, Abdelhadi Habeb

Abstract readConsensus StatementReview
In one paragraph

Review in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Nandu ThalangePediatric Endocrinologist, Genesis Healthcare, Dubai, United Arab Emirates.
Tawfeg Ben OmranMedical Geneticist, Sidra Medicine, Doha, Qatar.
Afaf AlsagheirPediatric Endocrinologist, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
Khalid HussainPediatric Endocrinologist, Sidra Medicine, Doha, Qatar.
Maha FadenMedical Geneticist and Metabolic Specialist, King Saud Medical City, Riyadh, Saudi Arabia.
Mona AglanProfessor of Clinical Genetics, National Research Centre, Cairo, Egypt.
Sareea AlremeithiPediatric Endocrinologist, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.
Abdelhadi HabebPediatric Endocrinologist, National Guard Hospital, Madinah, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Achondroplasia is the most common skeletal dysplasia and presents as a lifelong, multi-system condition characterized by disproportionate short stature, rhizomelic limb shortening, macrocephaly with frontal bossing, and a spectrum of neurological, respiratory, orthopedic, and psychosocial complications. Effective management requires anticipatory surveillance, coordinated multidisciplinary care, and early recognition of life-threatening complications. Therapeutic options have expanded in recent years with the introduction of vosoritide, a C-type natriuretic peptide analog that targets the underlying pathophysiology and has demonstrated significant improvements in linear growth and body proportionality in eligible children. However, global advances have not been uniformly translated into clinical practice across the Middle East, where challenges such as delayed diagnosis, inconsistent access to genetic testing, limited multidisciplinary infrastructure, and inequities in treatment availability continue to impact patient outcomes. In this document, a panel of pediatric endocrinologists and clinical geneticists from the Middle East convened to develop a set of regionally relevant, evidence-informed consensus statements on the diagnosis and management of achondroplasia in light of novel advances in the management of this condition. Using a modified Delphi process, the panel achieved consensus on 25 statements covering diagnosis, surveillance, multidisciplinary management, psychosocial support, pharmacologic interventions, transition to adult care, and research priorities. This consensus, endorsed by the Arab Society for Pediatric Endocrinology and Diabetes (ASPED) and the MENA Medical Genetics Association, aims to standardize and enhance the quality of care for individuals with achondroplasia across the region by integrating international best practices with local healthcare realities. The author panel believes that the implementation of these recommendations has the potential to improve early detection, optimize long-term outcomes, strengthen family support, and expand equitable access to emerging therapies.

Indexed as

AchondroplasiaDisease ManagementHumansMiddle EastFGFR3 testingmedical geneticsmiddle east guidelinespediatric endocrinologyskeletal dysplasiavosoritide

Identifiers

PMID42823987
PMCPMC13627016

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.