Familial congenital bilateral agenesis of the acromion: a radiologically illustrated case report

J J Hermans; E L Mooyaart; J G E Hendriks; R L Diercks

doi:10.1007/BF01631335

Familial congenital bilateral agenesis of the acromion: a radiologically illustrated case report

J J Hermans, E L Mooyaart, J G E Hendriks, R L Diercks

Onderzoeksoutput › Academic › peer review

2 Citaten (Scopus)

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Familial congenital bilateral acromion absence was found in four members of one family. Only one of them presented with gradually increasing pain in his left shoulder, resembling a shoulder impingement syndrome. The other members did not have any symptoms. This is the first report of familial occurrence of this extremely rare congenital anomaly.

Originele taal-2	English
Pagina's (van-tot)	337-339
Aantal pagina's	3
Tijdschrift	Surgical and radiologic anatomy
Volume	21
Nummer van het tijdschrift	5
DOI's	https://doi.org/10.1007/BF01631335
Status	Published - nov.-1999

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title = "Familial congenital bilateral agenesis of the acromion: a radiologically illustrated case report",

abstract = "Familial congenital bilateral acromion absence was found in four members of one family. Only one of them presented with gradually increasing pain in his left shoulder, resembling a shoulder impingement syndrome. The other members did not have any symptoms. This is the first report of familial occurrence of this extremely rare congenital anomaly.",

keywords = "Acromion/abnormalities, Adult, Aged, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Musculoskeletal Abnormalities/diagnostic imaging, Radiography, Shoulder Joint/diagnostic imaging",

author = "Hermans, {J J} and Mooyaart, {E L} and Hendriks, {J G E} and Diercks, {R L}",

year = "1999",

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doi = "10.1007/BF01631335",

language = "English",

volume = "21",

pages = "337--339",

journal = "Surgical and radiologic anatomy",

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T1 - Familial congenital bilateral agenesis of the acromion

T2 - a radiologically illustrated case report

AU - Hermans, J J

AU - Mooyaart, E L

AU - Hendriks, J G E

AU - Diercks, R L

PY - 1999/11

Y1 - 1999/11

N2 - Familial congenital bilateral acromion absence was found in four members of one family. Only one of them presented with gradually increasing pain in his left shoulder, resembling a shoulder impingement syndrome. The other members did not have any symptoms. This is the first report of familial occurrence of this extremely rare congenital anomaly.

AB - Familial congenital bilateral acromion absence was found in four members of one family. Only one of them presented with gradually increasing pain in his left shoulder, resembling a shoulder impingement syndrome. The other members did not have any symptoms. This is the first report of familial occurrence of this extremely rare congenital anomaly.

KW - Acromion/abnormalities

KW - Adult

KW - Aged

KW - Female

KW - Humans

KW - Magnetic Resonance Imaging

KW - Male

KW - Middle Aged

KW - Musculoskeletal Abnormalities/diagnostic imaging

KW - Radiography

KW - Shoulder Joint/diagnostic imaging

U2 - 10.1007/BF01631335

DO - 10.1007/BF01631335

M3 - Article

C2 - 10635098

SN - 0930-1038

VL - 21

SP - 337

EP - 339

JO - Surgical and radiologic anatomy

JF - Surgical and radiologic anatomy

IS - 5

ER -

Familial congenital bilateral agenesis of the acromion: a radiologically illustrated case report

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