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2 associated genes
32 signs/symptoms
COMMON GENES: 1
COMMON SIGNS: 4
1 OMIM reference -
1 associated gene
33 signs/symptoms
12q14 microdeletion syndrome
Buschke-Ollendorff syndrome

HMGA2 LEMD3
LEMD3


COMMON
GENES
LEMD3



Citations in the biomedical literature:


12q14 microdeletion syndrome
HMGA2 LEMD3
Buschke-Ollendorff syndrome



12q14 microdeletion syndrome
Buschke-Ollendorff syndrome

Synonym(s):
- Del(12)(q14)
- Deletion 12q14
- Monosomy 12q14
- Osteopoikilosis - short stature - intellectual deficit

Synonym(s):
- Disseminated dermatofibrosis with osteopoikilosis

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare skin disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: unknown
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C537415


COMMON
SIGNS
- Diabetes mellitus
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Short stature / dwarfism / nanism
- Subcutaneous nodules / lipomas / tumefaction / swelling


12q14 microdeletion syndrome
Buschke-Ollendorff syndrome

Very frequent
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Intrauterine growth retardation
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia

Frequent
- Abnormal pigmentary skin changes / skin pigmentation anomalies
- Tremor

Occasional
- Agenesis / hypoplasia / aplasia of kidneys
- Anodontia / oligodontia / hypodontia
- Arnold-Chiari anomaly
- Asplenia / polysplenia / spleen lobulation / accessory spleen
- Broad nose / nasal bridge
- Clinodactyly of fifth finger
- Deepset eyes / enophthalmos
- Downturned mouth
- Ectopic / horseshoe / fused kidneys
- Frontal bossing / prominent forehead
- High nasal bridge
- Hypotonia
- Intestinal / gut / bowel malrotation
- Micrognathia / retrognathia / micrognathism / retrognathism
- Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy
- Scoliosis
- Small / triangular nares / nostrils
- Synophris / synophrys
- Syringomelia
- Thick / bushy eyebrows
- Thin / retracted lips
- Triangular face


Very frequent
- Abnormal cry / voice / phonation disorder / nasal speech
- Abnormal dentition / dental position / implantation / unerupted / dental ankylosis
- Anomalies of bones / skeletal anomalies
- Autosomal dominant inheritance
- Bone pain
- Diffuse / generalised skin hypopigmentation / cutaneous albinism
- Epiphyseal anomaly
- Follicular / erythematous / edematous papules / milium
- Hearing loss / hypoacusia / deafness
- Hyperostosis
- Hypoplastic aorta / coarctation / stenosis / anomaly / aortic arch interruption
- Metaphyseal anomaly
- Nasal congestion / sinusitis / rhinitis / rhinorrhea
- Osteosclerosis / osteopetrosis / bone condensation
- Sarcoma
- Visual loss / blindness / amblyopia

Frequent
- Mediastinal / hilar adenopathies
- Strabismus / squint

Occasional
- Abnormal scarring / cheloids / hypertrophic scars
- Arthritis / synovitis / synovial proliferation
- Articular / joint pain / arthralgia
- Contractures / cramps / trismus / tetania / claudication / opisthotonos
- Diaphyseal anomaly
- Insulin-dependent / type 1 diabetes
- Lateral cleft lip / gingival cleft / paramedian nasal cleft
- Mutiple fractures / bone fragility
- Myalgia / muscular pain
- Palmoplantar hyperkeratosis / keratoderma
- Pigmented naevi / naevus pigmentosus / lentigo