ORPHA:2429
Macrocephaly-spastic paraplegia-dysmorphism syndrome
Also known as: Fryns macrocephaly
Publications
1
1.9th percentile
Trials
0
Interventional, condition-specific
Researchers
2
Distinct authors in sample
Gene link
—
Readiness
2/6
Stages with a signal
Clinical definition (Orphanet)
Macrocephaly-spastic paraplegia-dysmorphism syndrome is a rare syndrome of multiple anomalies characterized by macrocephaly (of post-natal onset) with large anterior fontanelle, complex spastic paraplegia, facial features (broad and high forehead, deeply set eyes, short philtrum with thin upper lip, large mouth and prominent incisors), , and intellectual deficit of varying severity. Inheritance appears to be .
How rare: How common this is has not been clearly measured.
Cross-references
Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.
- MONDO:0010858
- MeSH:C563963
- OMIM:600302
- UMLS:C1838281
Research stages
Trial readiness signals
Where this condition sits on an open-data research pipeline — not how close a treatment is, and not medical advice. Empty stages often mean “not in these databases under this Mondo ID,” not “impossible.”
2/6 stages with a signal
No specific-condition interventional trial, but broader-category trials exist — discuss eligibility with a clinician.
- Gene identifiedNot found
No GenCC disease–gene assertion in this build
- LiteraturePresent
1 matched papers (0 in last 10 years) Source
- Phenotype characterisedNot checked
Not yet enriched from Monarch / HPO
- Animal modelNot checked
Not yet enriched from Monarch / Alliance
- Orphan designationNot checked
FDA/EMA orphan-drug designation not enriched yet
- Interventional trialPartial
None under the specific name; 102 for broader category paraplegia
Biology
Genes and phenotypes
Gene–disease validity from GenCC, plus phenotypes and animal models joined from Monarch Initiative via Mondo ID — not a clinical diagnosis aid.
Do we know what causes it?
Not yet — the cause hasn't been pinned down in GenCC.
No strong gene–disease assertion joined for this Orphanet entity.
Phenotypes (Monarch / HPO)
Not enriched in this build — Monarch phenotype joins were not run for this record.
Animal models (Monarch / Alliance)
Not enriched in this build.
Literature
Is anyone studying this?
1
1 paper have ever been indexed under this name. For scale, breast cancer has over 700,000. Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=5449) is 41.
1 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 41 (publications denominator n=5449).
0 in the last 10 years · high confidence · 1.9th percentile (publications denominator)
Phrase hits: 1 · MeSH hits: 0
Who's working on it?
2
Distinct author names in 1 sampled paper — named people below.
Who's working on it?
No interventional trial matched this name; these authors publish on it in the sampled literature — a practical starting point for contact.
- 01Josephson KD1 paper · 2003Papers in Europe PMC
- 02Williams MS1 paper · 2003
Department of Pediatrics, Gundersen Lutheran Medical Center LaCrosse, Wisconsin 54601, USA. mswillia@gundluth.org
Papers in Europe PMC
Clinical research
Is a treatment being tested?
0
interventional trials for this specific condition
No interventional trial testing a treatment matched this specific condition name on ClinicalTrials.gov (observational studies and pan-disease registries are listed separately when present). 102 trials are registered for paraplegia, the broader category — shown separately because they may or may not enrol this specific subtype.
Data as of 27 July 2026
No matched interventional trials. This is true for 73% of diseases in the trials denominator (5114 of 7003). Here are the researchers publishing on it.
high confidence · 36.5th percentile (trials denominator)
Recruiting interventional trials
From the matched ClinicalTrials.gov set
No interventional trial testing a treatment was found for this specific condition name on ClinicalTrials.gov.
102 interventional trials matched paraplegia, the broader category — listed below. Those studies are not counted in the condition-specific total.
Broader category: paraplegia
102
Interventional trials for the parent category, exclusive of NCT IDs already counted above. Eligibility for this subtype is not guaranteed.
Worth raising with a clinician. How we count trials.
Recruiting under the broader category
- NCT06295146·RECRUITING·Virtual Peer Coaching in Manual Wheelchair Skills
Conditions: Wheelchair · Paraplegia · Spinal Cord Injury · Tetraplegia/Tetraparesis·Matched via name phrase
- NCT06829212·RECRUITING·Research on Wireless Brain Implant System for General Control of External Devices
Conditions: Complete or Incomplete Paraplegia/quadriplegia · Spinal Cord Injury · Brainstem Stroke · Amyotrophic Lateral Sclerosis·Matched via name phrase
- NCT07536386·RECRUITING·Self-balancing Personal Exoskeleton for SCI (WIP)
Conditions: Spinal Cord Injuries · Paraplegia and Tetraplegia·Matched via name phrase
- NCT07583576·NOT YET RECRUITING·Effects of Functional Electrical Stimulation on Spasticity, Quadriceps Muscle Strength and Functional Mobility in Individuals With Paraplegia
Conditions: Spinal Cord Injury · Paraplegia · Spasticity · Neurorehabilitation·Matched via name phrase
- NCT07561359·ENROLLING BY INVITATION·12-Week Strength and Functional Exercise Program for Hereditary Spastic Paraplegia Trial (HSPMOVE)
Conditions: Hereditary Spastic Paraplegia·Matched via name phrase
- NCT07417943·RECRUITING·Neuromodulation to Enhance Motor Function in HSP
Conditions: Hereditary Spastic Paraplegia·Matched via name phrase
- NCT06261424·RECRUITING·Effects of a Supervised Rehabilitation Program on Disease Severity in Spastic Ataxias
Conditions: Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay · Spastic Paraplegia 7·Matched via name phrase
- NCT07136844·RECRUITING·Gait Analysis Parameter and Upper Limb Evaluation in Adult Patients With Neurological or Metabolic Pathology
Conditions: Neuromuscular Diseases · Obesity (Disorder) · Myotonic Dystrophy 1 · Myasthenic Syndrome·Matched via name phrase
- NCT01474148·RECRUITING·A Neuroprosthesis for Seated Posture and Balance
Conditions: Spinal Cord Injury · Paralysis · Tetraplegia · Paraplegia·Matched via name phrase
- NCT03206190·RECRUITING·The preSPG4 Study - Studying the Prodromal and Early Phase of SPG4
Conditions: Hereditary Spastic Paraplegia · Hereditary, Spastic Paraplegia, Autosomal Dominant·Matched via name phrase
- NCT06742697·RECRUITING·Flexibility, Resistance, Aerobic, Movement Execution Training in Adults With Hereditary Spastic Paraplegia
Conditions: Hereditary Spastic Paraplegia·Matched via name phrase
- NCT05518188·RECRUITING·Melpida: Recombinant Adeno-associated Virus (Serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt)
Conditions: Spasticity, Muscle · Microcephaly · Intellectual Deficiency · Growth Retardation·Matched via name phrase
- NCT06272279·RECRUITING·Neuromodulation With Spinal Stimulation Methods
Conditions: Spinal Cord Injuries · Spinal Cord Injury at C5-C7 Level · Paraplegia, Spinal · Paraplegia, Incomplete·Matched via name phrase
- NCT03225625·ENROLLING BY INVITATION·Stem Cell Spinal Cord Injury Exoskeleton and Virtual Reality Treatment Study
Conditions: Spinal Cord Injuries · Spinal Cord Compression · Spinal Cord Ischemia · Spinal Cord Diseases·Matched via name phrase
- NCT03026816·RECRUITING·Epidural Stimulation After Neurologic Damage
Conditions: Spinal Cord Injuries · Paraplegia, Complete·Matched via name phrase
Where to find support
We do not yet link condition-specific patient organisations. These umbrella groups support undiagnosed and ultra-rare families:
India — NPRD
Last verified 2026-07-26This ORPHAcode is not on our curated NPRD list (direct or Mondo-parent match). That does not decide clinical eligibility; families in India should ask a notified Centre of Excellence about current coverage.
Hand-curated for this project. ORPHAcode mappings are best-effort and may be incomplete or imprecise for umbrella categories. Parent (Mondo) matches mean the policy lists a broader category — confirm eligibility with a Centre of Excellence. Financial entitlements summarised from public policy statements and may change. This is not official government guidance.
How we counted this
Europe PMC query (preferred label + any corrected label + Orphanet and Mondo exact synonyms, stoplisted; unioned with resolved MeSH labels when available). UMLS / OMIM / NCIT cross-references are stored on the overview but are not added to the query string.
"Macrocephaly-spastic paraplegia-dysmorphism syndrome" OR "Fryns macrocephaly"
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Macrocephaly-spastic paraplegia-dysmorphism syndrome" OR "Fryns macrocephaly"
Study-type breakdown: 0 interventional · 0 observational · 0 expanded access. Only interventional studies enter the trial headline.
Parent-category trials query:
"paraplegia"
Query health: ok — strategies attempted: phrase; with hits: phrase
Run this search on ClinicalTrials.gov
Confidence reasoning
- Preferred label is multi-word and distinctive
- No synonyms dropped by stoplist
- No label/synonym collisions with other diseases in this corpus
Ingested 2026-07-26T20:08:58.464Z
