National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome


Other Names:
Mandibular hypoplasia, deafness, progeroid features; Mandibular hypoplasia-deafness-progeroid syndrome; Mandibular hypoplasia-hearing loss-progeroid syndrome; Mandibular hypoplasia, deafness, progeroid features; Mandibular hypoplasia-deafness-progeroid syndrome; Mandibular hypoplasia-hearing loss-progeroid syndrome; Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome; MDPL syndrome; MDP syndrome See More
The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs.
orphanet

Orpha Number: 363649

Definition
Mandibular hypoplasia-deafness-progeroid syndrome is a rare, genetic, premature aging disease characterized by sensorineural deafness, generalized lack of subcutaneous fatty tissue (although with increased truncal deposition) noted from childhood, scleroderma, and facial dysmorphism which includes prominent eyes, a beaked nose, small mouth, crowded teeth and mandibular hypoplasia. Other associated features include growth delay, joint contractures, telangiectasia, hypogonadism (with lack of breast development in females), cryptorchidism, skeletal muscle atrophy, hypertriglycemia and diabetes mellitus/insulin resistance.

Visit the Orphanet disease page for more resources.
Last updated: 7/1/2018

This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.

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Medical Terms Other Names
Learn More:
HPO ID
Percent of people who have these symptoms is not available through HPO
Autosomal dominant inheritance 0000006
Convex nasal ridge
Beaked nose
Beaklike protrusion
Hooked nose
Polly beak nasal deformity
[ more ] 		0000444
Cryptorchidism
Undescended testes
Undescended testis
[ more ] 		0000028
Dental crowding
Crowded teeth
Dental overcrowding
Overcrowding of teeth
[ more ] 		0000678
Dermal atrophy
Skin degeneration
0004334
Diabetes mellitus 0000819
Elevated hepatic transaminase
High liver enzymes
0002910
Flexion contracture
Flexed joint that cannot be straightened
0001371
Hepatic steatosis
Fatty infiltration of liver
Fatty liver
[ more ] 		0001397
Hepatomegaly
Enlarged liver
0002240
High pitched voice 0001620
Hypertriglyceridemia
Increased plasma triglycerides
Increased serum triglycerides
Increased triglycerides
[ more ] 		0002155
Hypogonadism
Decreased activity of gonads
0000135
Insulin resistance
Body fails to respond to insulin
0000855
Kyphosis
Hunched back
Round back
[ more ] 		0002808
Lack of skin elasticity 0100679
Lipodystrophy
Inability to make and keep healthy fat tissue
0009125
Micrognathia
Little lower jaw
Small jaw
Small lower jaw
[ more ] 		0000347
Narrow mouth
Small mouth
0000160
Osteoporosis 0000939
Proptosis
Bulging eye
Eyeballs bulging out
Prominent eyes
Prominent globes
Protruding eyes
[ more ] 		0000520
Scleroderma 0100324
Scoliosis 0002650
Sensorineural hearing impairment 0000407
Telangiectasia 0001009
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Last updated: 7/1/2020

These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.

In-Depth Information

  • Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome. Click on the link to view a sample search on this topic.

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