> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/condition/adult-syndrome-8aeb5e11-f165-5276-850c-05129a3e72a5
> Record changed: 2026-10-13

# ADULT syndrome

Therapeutic area

Dermatology

Rare disease

Yes

## Definition and classification

**Definition**

ADULT (Acro-dermo-ungual-lacrimal-tooth) syndrome is a rare ectodermal dysplasia syndrome characterized by ectrodactyly, syndactyly, mammary hypoplasia, and excessive freckling as well as other typical ectodermal defects such as hypodontia, lacrimal duct anomalies, hypotrichosis, and onychodysplasia.

**Genetic basis**

Yes

**Non-human condition**

No

**Rare disease**

Yes

**Listing at source**

Listed

**Condition name**

ADULT syndrome

**Therapeutic area**

Dermatology

### Alternative names (6)

- ADULT syndrome
- ADULT syndrome
- acro-dermato-ungual-lacrimal-tooth syndrome
- acrodermatounguallacrimaltooth syndrome
- pigment anomaly-ectrodactyly-hypodontia syndrome
- acro dermato ungual lacrimal tooth syndrome

## Clinical profile

**Severity**

Moderate

### Disease mechanisms (4)

- Developmental
- Genetic
- Hereditary
- Syndromic

### All therapeutic areas (2)

- Dermatology
- Rheumatology

## Identifiers

**MONDO ID**

MONDO:0007072

Source: [monarchinitiative.org](https://monarchinitiative.org/MONDO:0007072)

**Parent condition**

MONDO:0000426

## Related records

### Broader conditions (24)

- Autosomal dominant disease
- Autosomal genetic disease
- Bone development disease
- [Bone disorder](https://trialight.com/data/condition/bone-disorder-83c4c003-c8df-50f7-8829-fbbb5d5adf76.md)
- Congenital limb malformation
- Developmental defect during embryogenesis
- Disease
- Disease by body system or component
- Disease by developmental or physiological process
- Disease by etiologic mechanism
- Disease of genetic or genomic mechanism
- Disorder of development or morphogenesis
- Dysostosis
- Ectodermal dysplasia syndrome
- Hereditary disease
- Hereditary epidermal appendage anomaly
- [Hereditary skin disorder](https://trialight.com/data/condition/hereditary-skin-disorder-f5d8c433-73e1-52b2-8b9a-f3ca836efe24.md)
- Human disease
- Integumentary system disorder
- Musculoskeletal system disorder

### Trials (604)

- 11C-YJH08 PET Imaging for Detection of Glucocorticoid Receptor Expression
- 177Lu-DTPA-Omburtamab Radioimmunotherapy for Leptomeningeal Metastasis From Solid Tumors (Breast, NSCLC, Malignant Melanoma)
- 18F-FDG Uptake Measurements in Malignant Solid Tumors on PET/CT and PET/MR
- 18F-Fluciclovine PET Amino Acid Evaluation of Brain Metastasis Treated With Stereotactic Radiosurgery
- 3D011-08 Monotherapy in Subjects With Advanced Solid Tumors
- 64Cu-GRIP B in Patients With Advanced Malignancies
- 68 Gallium-Fibroblast Activating Protein Inhibitors-46 Positron Emission Tomography - Computerized Tomography for Molecular Assessment of Fibroblast Activation and Risk Assessment in Solid Tumors
- 89Zr-KN035 PET Imaging in Patients With Advanced Solid Tumors
- 89Zr-labeled KN035 PET Imaging in Patients With PD-L1 Positive Solid Tumors
- A Beta-only IL-2 ImmunoTherapY Study
- A Biospecimen Collection Study of Leukapheresis-Derived Circulating Tumor Cells, Immune Cells, and Progenitor Cells.
- A Clinical Study on the Efficacy and Mechanism of Tumor Treatment Vaccine (TTV) for Recurrent and Refractory Advanced Solid Tumors
- A Clinical Study to Evaluate CAR-T Cell-based Medicinal Product in the Treatment of Advanced Solid Tumors
- A Clinical Study to Evaluate the Safety, Tolerability and Efficacy of IOS-1002 Administered Alone and in Combination With Pembrolizumab, a PD-1 Monoclonal Antibody in Advanced Solid Tumors
- A Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of HLX26 Monoclonal Antibody Injection in Patients With Solid Tumor or Lymphoma
- a Feasibility Study of iHD-SRT for BM
- A First in Human Study of AUR 103 Calcium to Evaluate Safety, Pharmacokinetics and Pharmacodynamics
- A First-in-human Study of 3HP-2827 in Patients With Unresectable or Metastatic Solid Tumors With FGFR2 Alterations
- A First-in-Human Study of JAB-8263 in Adult Patients With Advanced Solid Tumors
- A Long-Term Follow-Up Study of Participants Treated With A2 Biotherapeutics (A2 Bio) Gene Therapy (GT) Products

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