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An ectodermal dysplasia syndrome characterized by the association of abnormalities of the eyelids, lips, and teeth.
No HPO annotations are available for this condition.
Diffuse gastric and lobular breast cancer syndrome (DGLBCS) is characterized by an increased risk of diffuse gastric cancer (DGC) and lobular breast cancer (LBC). Cleft lip with or without cleft palate has been reported in some individuals with CDH1-related DGLBCS. Table 2. Diffuse Gastric and Lobular Breast Cancer Syndrome: Frequency of Select Features
Feature | Frequency of Feature by Gene | Comment |
|---|---|---|
CTNNA1 Diffuse gastric cancer | 10%-70% of males1,27%-56% of females1,2 | 49%-57%3 |
Lobular breast cancer | 37%-42% of females1,4 | NR |
Cleft lip ± cleft palate | 3%5 | NR |
Source: GeneReviews — "Diffuse Gastric and Lobular Breast Cancer Syndrome"
Consensus genetic testing criteria for diffuse gastric and lobular breast cancer syndrome (DGLBCS), also known as hereditary diffuse gastric cancer (HDGC), have been published .
DGLBCS should be suspected in a proband with ANY of the following clinical features or family history :
Clinical features
Source: GeneReviews — "Diffuse Gastric and Lobular Breast Cancer Syndrome"
An estimated 5%-10% of all gastric cancers are thought to present familial clustering ; only a small fraction of gastric cancers are believed to be hereditary and explained by a genetic cause. Identification of individuals at risk for diffuse gastric and lobular breast cancer syndrome (DGLBCS) is complicated by several factors: • DGLBCS is one of several hereditary cancer syndromes characterized by gastric and breast cancer and associated premalignant lesions. • Risk of a hereditary cancer syndrome with an overlapping tumor spectrum may not be apparent in an individual with an unknown/unreported family history presenting with isolated gastric or breast cancer detected at early age . Detailed histologic classification of gastric (diffuse vs non-diffuse) and breast (lobular vs non-lobular) cancers is necessary to identify individuals and families at risk for DGLBCS and to facilitate appropriate genetic testing. Cancer predisposition syndromes that include gastric and/or breast cancer as part of their disease spectrum (despite not being the primary associated cancers) are listed in . Table 4. Cancer Predisposition Syndromes in the Differential Diagnosis of Diffuse Gastric and Lobular Breast Cancer Syndrome
Gene(s) | Disorder | MOI |
|---|
No approved treatments are currently available for blepharocheilodontic syndrome. The disease remains an area of unmet medical need.
Clinical practice guidelines for diffuse gastric and lobular breast cancer syndrome (DGLBCS) have been published .
To establish the extent of disease and needs in an individual diagnosed with DGLBCS, the evaluations summarized (if not performed as part of the evaluation that led to the diagnosis) are recommended.
Table 5.
Diffuse Gastric and Lobular Breast Cancer Syndrome: Recommended Evaluations Following Initial Diagnosis
System/Concern | Evaluation | Comment
| • Referral to a DGC center of expertise for screening
Endoscopy w/multiple gastric biopsies to assess for macroscopic tumor microscopic pre-malignant or malignant lesions
Eval for H pylori infection given its major role as risk factor in gastric carcinogenesis1
| • For those w/CDH1 pathogenic variant or CTNNA1 truncating pathogenic variant, beginning in early adulthood or 5-10 yrs prior to earliest gastric cancer diagnosis in family w/minimum age of 18 yrs
For those w/suspected DGLBCS of unknown cause, beginning at age 40 yrs or 5-10 yrs prior to earliest gastric cancer case in family, w/minimum age of 18 yrs
| In females:
Referral to high-risk breast cancer clinic
Clinical breast exam in those age ≥20 yrs
Breast MRI in those age 30-40 yrs
Breast MRI combined w/mammography in those age ≥40 yrs
| • Mammography alone is inadequate to identify LBC; if MRI is unavailable, consider incl breast ultrasound.
Source: GeneReviews — "Diffuse Gastric and Lobular Breast Cancer Syndrome"
Clinical trials, targeted therapies, and predictive markers of therapy response directed to DGC or LBC are scarce. Ongoing studies are mainly investigating alternate medication doses and combining therapeutic agents that are approved for sporadic gastric cancer and other solid tumors (e.g., platinum compounds, fluropyrimidines, and topoisomerase I inhibitors). Immunotherapy for anti-HER2, anti-VEGDR2, and anti-PD1 have been approved for treatment of gastric adenocarcinoma; however, treatment data for DGC is weak. The MONO study (NCT01197885), a Phase II clinical trial, examined the outcome of zolbetuximab (monoclonal antibody against CLDN18.2: IMAB362) monotherapy in a series of individuals with recurrent or refractory, locally advanced or metastatic, CLDN18.
Source: GeneReviews — "Diffuse Gastric and Lobular Breast Cancer Syndrome"
1 trial found
To monitor existing manifestations, the individual's response to supportive care, and the emergence of new manifestations, the evaluations summarized (individuals with CDH1- or CTNNA1-related DGLBCS) and 7b (individuals with DGLBCS of unknown genetic cause) are recommended.
Table 7a.
CDH1- or CTNNA1-Related Diffuse Gastric and Lobular Breast Cancer Syndrome: Recommended Surveillance
System/Concern | Evaluation | Frequency
| Referral to high-risk gastric cancer screening program |
Upper endoscopy to incl:
Thorough ≥30-minute exam
Targeted biopsies of all suspicious lesions
Followed by random biopsies from specific anatomic regions using IGCLC Cambridge1 or Bethesda method2,3
Note: Endoscopy permits direct inspection biopsy of suspicious areas; however, DGC tends to spread in submucosa, where lesions are difficult to identify. | • Every 6-12 mos beginning at age 40 yrs (or 5-10 yrs prior to earliest gastric cancer diagnosis in family), w/minimum age of 18 yrs
Note: (1) For individuals w/unclear risk of DGC, the interval between endoscopies can be increased after 2 consecutive normal endoscopies at discretion of a DGC specialist based on endoscopy findings family history. (2) Choosing endoscopy surveillance vs prophylactic gastrectomy is challenging; it is difficult to determine if intramucosal lesions identified on endoscopy will remain indolent /or become aggressive.
Source: GeneReviews — "Diffuse Gastric and Lobular Breast Cancer Syndrome"
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
1 clinical trial registered. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.
5 publications have been identified in PubMed for blepharocheilodontic syndrome. Research spans Case Report / Case Series (60%), Basic Science / Preclinical (20%), and Epidemiology / Natural History (20%).
Vaessen C (2026). [PMID: 41517846](https://pubmed.ncbi.nlm.nih.gov/41517846/). *Journal of gastric cancer*. [Epidemiology / Natural History]
Rejaey A (2026). [PMID: 41563506](https://pubmed.ncbi.nlm.nih.gov/41563506/). *Archives of gynecology and obstetrics*. [Case Report / Case Series]
Loughman L (2025). [PMID: 40028877](https://pubmed.ncbi.nlm.nih.gov/40028877/). *American journal of medical genetics. Part A*. [Case Report / Case Series]
Sidhu AS (2025). [PMID: 39442179](https://pubmed.ncbi.nlm.nih.gov/39442179/). *Orbit (Amsterdam, Netherlands)*. [Case Report / Case Series]
Gossner L (2024). [PMID: 39596675](https://pubmed.ncbi.nlm.nih.gov/39596675/). *Genes*. [Basic Science / Preclinical]
Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 12:30 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Features of Disorder Distinguishing from DGLBCS |
|---|
APC-assoc polyposis conditions | AD | Gastric cancer | Gastric cancer often differs histologically from DGC.; CRC is the most commonly assoc cancer.; Adenomatous gastrointestinal polyps; Additional physical features (dental anomalies, CHRPE, osteomas) BMPR1A SMAD4 | — |
Juvenile polyposis syndrome | AD | Gastric cancer | Gastrointestinal polyposis BRCA1 BRCA2 | — |
BRCA1- BRCA2-assoc hereditary breast ovarian cancer | AD | Breast cancer; Gastric cancer1 | Risk of other cancers (ovarian, prostate, pancreatic, melanoma) MAX SDHA SDHAF2 SDHB SDHC SDHD TMEM127 | — |
Hereditary paraganglioma-pheochromocytoma syndromes | AD | Gastric cancer | GIST; Risk of other cancers (paragangliomas, pheochromocytomas, renal clear cell); Pulmonary chondromas MLH1 MSH2 MSH6 PMS2 EPCAM | — |
Lynch syndrome | AD | Gastric cancer (≤20% is DGC in those w/Lynch syndrome)2; Breast cancer3 | Gastric cancer often differs histologically from DGC.; CRC is the most commonly assoc cancer.; Risk of other cancers (endometrium, ovary, stomach, small bowel, urinary tract, biliary tract, brain) MUTYH | — |
MUTYH polyposis | AR | Gastric cancer | Colonic adenomatous polyps; CRC is the most commonly assoc cancer. | — |
PALB2 | PALB2-related hereditary breast ovarian cancer (OMIM 620442) | AD | Gastric cancer; Breast cancer | Risk of other cancers (ovarian pancreas) PTEN |
Source: GeneReviews — "Diffuse Gastric and Lobular Breast Cancer Syndrome"