Ehlers-Danlos syndrome type 7A

General Information (adopted from Orphanet):

Synonyms, Signs: EDS7B, INCLUDED
EDS VII, MUTANT PROCOLLAGEN TYPE EDS VIIB, INCLUDED
ARTHROCHALASIS MULTIPLEX CONGENITA
EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE
EDS VIIA
EDS7A
Number of Symptoms 26
OrphanetNr: 99875
OMIM Id: 130060
ICD-10: Q79.6
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant
[Orphanet]
Age of onset: Neonatal
Infancy
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Ehlers-Danlos syndrome, arthrochalasic type
 -Rare developmental defect during embryogenesis
 -Rare genetic disease
 -Rare skin disease
 -Rare systemic or rheumatologic disease

Symptom Information: Sort by abundance 

1
(HPO:0011800) Midface retrusion 221 / 7739
2
(HPO:0002194) Delayed gross motor development 37 / 7739
3
(HPO:0008780) Congenital bilateral hip dislocation 4 / 7739
4
(HPO:0002808) Kyphosis 289 / 7739
5
(HPO:0003088) Premature osteoarthritis 10 / 7739
6
(HPO:0000938) Osteopenia 138 / 7739
7
(HPO:0002650) Scoliosis 705 / 7739
8
(HPO:0001382) Joint hypermobility Very frequent [Orphanet] 231 / 7739
9
(HPO:0001623) Breech presentation 16 / 7739
10
(HPO:0004322) Short stature Very frequent [Orphanet] 1232 / 7739
11
(HPO:0001058) Poor wound healing 9 / 7739
12
(HPO:0000963) Thin skin Very frequent [Orphanet] 96 / 7739
13
(HPO:0000974) Hyperextensible skin Very frequent [Orphanet] 59 / 7739
14
(HPO:0000987) Atypical scarring of skin Very frequent [Orphanet] 58 / 7739
15
(HPO:0001075) Atrophic scars 15 / 7739
16
(HPO:0000978) Bruising susceptibility 123 / 7739
17
(HPO:0010547) Muscle flaccidity 466 / 7739
18
(HPO:0001252) Muscular hypotonia 990 / 7739
19
(HPO:0008947) Infantile muscular hypotonia 482 / 7739
20
(HPO:0001324) Muscle weakness Very frequent [Orphanet] 859 / 7739
21
(OMIM) Recurrent joint subluxation 3 / 7739
22
(OMIM) Joint laxity, severe 3 / 7739
23
(MedDRA:10017322) Fractures 18 / 7739
24
(OMIM) Mild to moderate short stature 7 / 7739
25
(OMIM) Thin, velvety skin 3 / 7739
26
(MedDRA:10017076) Fracture 18 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Description: (OMIM) EDS type VII is distinguished from the other types of EDS by the frequency of congenital hip dislocation and extreme joint laxity with recurrent joint subluxations and minimal skin involvement (Byers et al., 1997; Giunta et al., 2008). ...
Clinical Description OMIM Lichtenstein et al. (1973) reported a patient with arthrochalasis multiplex congenita, including short stature, small mandible, considerable hyperextensibility, and increased skin bruising. Although the patient was originally thought to have deficiency of procollagen proteinase, Steinmann et al. (1980) ...
Molecular genetics OMIM In a girl with EDS VIIA reported by Cole et al., 1986), Weil et al. (1989) identified a de novo heterozygous mutation in the COL1A1 gene that resulted in the skipping of exon 6 (120150.0026). The deleted peptides ...