Mandibuloacral dysplasia progeroid syndrome
Summary
Clinical features
Help- Abnormality of blood and blood-forming tissues
- Elevated hemoglobin A1c
Elevated hemoglobin A1c
- MedGen UID: 892798
- Concept ID: C4073162
- Finding: Finding
Abnormality of blood and blood-forming tissues
- Elevated hemoglobin A1c
- Abnormality of head or neck
- Bulbous nose
Bulbous nose
- MedGen UID: 66013
- Concept ID: C0240543
- Finding: Finding
Abnormality of head or neck
- Depressed nasal bridge
Depressed nasal bridge
- MedGen UID: 373112
- Concept ID: C1836542
- Finding: Finding
Abnormality of head or neck
- High forehead
High forehead
- MedGen UID: 65991
- Concept ID: C0239676
- Finding: Finding
Abnormality of head or neck
- High palate
High palate
- MedGen UID: 66814
- Concept ID: C0240635
- Finding: Congenital Abnormality
Abnormality of head or neck
- Intra-oral hyperpigmentation
Intra-oral hyperpigmentation
- MedGen UID: 585590
- Concept ID: C0399483
- Finding: Finding
Abnormality of head or neck
- Long philtrum
Long philtrum
- MedGen UID: 351278
- Concept ID: C1865014
- Finding: Finding
Abnormality of head or neck
- Narrow mouth
Narrow mouth
- MedGen UID: 44435
- Concept ID: C0026034
- Finding: Congenital Abnormality
Abnormality of head or neck
- Narrow nasal ridge
Narrow nasal ridge
- MedGen UID: 373404
- Concept ID: C1837761
- Finding: Finding
Abnormality of head or neck
- Partial congenital absence of teeth
Partial congenital absence of teeth
- MedGen UID: 43794
- Concept ID: C0020608
- Finding: Congenital Abnormality
Abnormality of head or neck
- Short philtrum
Short philtrum
- MedGen UID: 350006
- Concept ID: C1861324
- Finding: Finding
Abnormality of head or neck
- Sparse eyebrow
Sparse eyebrow
- MedGen UID: 371332
- Concept ID: C1832446
- Finding: Finding
Abnormality of head or neck
- Triangular face
Triangular face
- MedGen UID: 324383
- Concept ID: C1835884
- Finding: Finding
Abnormality of head or neck
- Underdeveloped nasal alae
Underdeveloped nasal alae
- MedGen UID: 322332
- Concept ID: C1834055
- Finding: Congenital Abnormality
Abnormality of head or neck
- Bulbous nose
- Abnormality of limbs
- Acroosteolysis
Acroosteolysis
- MedGen UID: 183017
- Concept ID: C0917990
- Finding: Disease or Syndrome
Abnormality of limbs
- Decreased fibular diameter
Decreased fibular diameter
- MedGen UID: 1383699
- Concept ID: C4476976
- Finding: Finding
Abnormality of limbs
- Deep palmar crease
Deep palmar crease
- MedGen UID: 387849
- Concept ID: C1857539
- Finding: Finding
Abnormality of limbs
- Dysplasia of the femoral head
Dysplasia of the femoral head
- MedGen UID: 866895
- Concept ID: C4021251
- Finding: Finding
Abnormality of limbs
- Genu valgum
Genu valgum
- MedGen UID: 154364
- Concept ID: C0576093
- Finding: Anatomical Abnormality
Abnormality of limbs
- Palmoplantar keratosis
Palmoplantar keratosis
- MedGen UID: 44017
- Concept ID: C0022596
- Finding: Disease or Syndrome
Abnormality of limbs
- Sandal gap
Sandal gap
- MedGen UID: 374376
- Concept ID: C1840069
- Finding: Finding
Abnormality of limbs
- Acroosteolysis
- Abnormality of metabolism/homeostasis
- Elevated circulating hepatic transaminase concentration
Elevated circulating hepatic transaminase concentration
- MedGen UID: 338525
- Concept ID: C1848701
- Finding: Finding
Abnormality of metabolism/homeostasis
- Glucose intolerance
Glucose intolerance
- MedGen UID: 75760
- Concept ID: C0271650
- Finding: Disease or Syndrome
Abnormality of metabolism/homeostasis
- Hypertriglyceridemia
Hypertriglyceridemia
- MedGen UID: 167238
- Concept ID: C0813230
- Finding: Finding
Abnormality of metabolism/homeostasis
- Elevated circulating hepatic transaminase concentration
- Abnormality of the cardiovascular system
- Left ventricular hypertrophy
Left ventricular hypertrophy
- MedGen UID: 57442
- Concept ID: C0149721
- Finding: Disease or Syndrome
Abnormality of the cardiovascular system
- Mitral regurgitation
Mitral regurgitation
- MedGen UID: 7670
- Concept ID: C0026266
- Finding: Disease or Syndrome
Abnormality of the cardiovascular system
- Mitral valve calcification
Mitral valve calcification
- MedGen UID: 181575
- Concept ID: C0919718
- Finding: Disease or Syndrome
Abnormality of the cardiovascular system
- Patent foramen ovale
Patent foramen ovale
- MedGen UID: 8891
- Concept ID: C0016522
- Finding: Congenital Abnormality
Abnormality of the cardiovascular system
- Tricuspid regurgitation
Tricuspid regurgitation
- MedGen UID: 11911
- Concept ID: C0040961
- Finding: Disease or Syndrome
Abnormality of the cardiovascular system
- Left ventricular hypertrophy
- Abnormality of the digestive system
- Hepatomegaly
Hepatomegaly
- MedGen UID: 42428
- Concept ID: C0019209
- Finding: Finding
Abnormality of the digestive system
- Macrovesicular hepatic steatosis
Macrovesicular hepatic steatosis
- MedGen UID: 373290
- Concept ID: C1837256
- Finding: Finding
Abnormality of the digestive system
- Hepatomegaly
- Abnormality of the eye
- Proptosis
Proptosis
- MedGen UID: 41917
- Concept ID: C0015300
- Finding: Disease or Syndrome
Abnormality of the eye
- Proptosis
- Abnormality of the genitourinary system
- Focal segmental glomerulosclerosis
Focal segmental glomerulosclerosis
- MedGen UID: 4904
- Concept ID: C0017668
- Finding: Disease or Syndrome
Abnormality of the genitourinary system
- Proteinuria
Proteinuria
- MedGen UID: 10976
- Concept ID: C0033687
- Finding: Finding
Abnormality of the genitourinary system
- Focal segmental glomerulosclerosis
- Abnormality of the integument
- Nail dystrophy
Nail dystrophy
- MedGen UID: 66368
- Concept ID: C0221260
- Finding: Disease or Syndrome
Abnormality of the integument
- Poikiloderma
Poikiloderma
- MedGen UID: 97905
- Concept ID: C0392777
- Finding: Disease or Syndrome
Abnormality of the integument
- Progeroid facial appearance
Progeroid facial appearance
- MedGen UID: 341830
- Concept ID: C1857710
- Finding: Finding
Abnormality of the integument
- Sparse hair
Sparse hair
- MedGen UID: 1790211
- Concept ID: C5551005
- Finding: Finding
Abnormality of the integument
- Nail dystrophy
- Abnormality of the musculoskeletal system
- Brachycephaly
Brachycephaly
- MedGen UID: 113165
- Concept ID: C0221356
- Finding: Congenital Abnormality
Abnormality of the musculoskeletal system
- Delayed cranial suture closure
Delayed cranial suture closure
- MedGen UID: 75805
- Concept ID: C0277828
- Finding: Finding
Abnormality of the musculoskeletal system
- Flexion contracture
Flexion contracture
- MedGen UID: 83069
- Concept ID: C0333068
- Finding: Anatomical Abnormality
Abnormality of the musculoskeletal system
- Frontal bossing
Frontal bossing
- MedGen UID: 67453
- Concept ID: C0221354
- Finding: Congenital Abnormality
Abnormality of the musculoskeletal system
- Generalized hypotonia
Generalized hypotonia
- MedGen UID: 346841
- Concept ID: C1858120
- Finding: Finding
Abnormality of the musculoskeletal system
- Generalized lipodystrophy
Generalized lipodystrophy
- MedGen UID: 1369615
- Concept ID: C4317112
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- J-shaped sella turcica
J-shaped sella turcica
- MedGen UID: 381480
- Concept ID: C1854718
- Finding: Finding
Abnormality of the musculoskeletal system
- Joint stiffness
Joint stiffness
- MedGen UID: 56403
- Concept ID: C0162298
- Finding: Sign or Symptom
Abnormality of the musculoskeletal system
- Micrognathia
Micrognathia
- MedGen UID: 44428
- Concept ID: C0025990
- Finding: Congenital Abnormality
Abnormality of the musculoskeletal system
- Osteopenia
Osteopenia
- MedGen UID: 18222
- Concept ID: C0029453
- Finding: Disease or Syndrome
Abnormality of the musculoskeletal system
- Pectus excavatum
Pectus excavatum
- MedGen UID: 781174
- Concept ID: C2051831
- Finding: Finding
Abnormality of the musculoskeletal system
- Shallow orbits
Shallow orbits
- MedGen UID: 351328
- Concept ID: C1865244
- Finding: Finding
Abnormality of the musculoskeletal system
- Short femoral neck
Short femoral neck
- MedGen UID: 373033
- Concept ID: C1836184
- Finding: Finding
Abnormality of the musculoskeletal system
- Supernumerary ribs
Supernumerary ribs
- MedGen UID: 83380
- Concept ID: C0345397
- Finding: Congenital Abnormality
Abnormality of the musculoskeletal system
- Thin ribs
Thin ribs
- MedGen UID: 98095
- Concept ID: C0426818
- Finding: Finding
Abnormality of the musculoskeletal system
- Brachycephaly
- Abnormality of the nervous system
- Abnormally high-pitched voice
Abnormally high-pitched voice
- MedGen UID: 66836
- Concept ID: C0241703
- Finding: Finding
Abnormality of the nervous system
- Abnormally high-pitched voice
- Growth abnormality
- Postnatal growth retardation
Postnatal growth retardation
- MedGen UID: 395343
- Concept ID: C1859778
- Finding: Finding
Growth abnormality
- Short stature
Short stature
- MedGen UID: 87607
- Concept ID: C0349588
- Finding: Finding
Growth abnormality
- Postnatal growth retardation
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.