Familial Parry-Romberg disease

Peter J. Anderson; Darren Molony; Eric Haan; David J. David

doi:10.1016/j.ijporl.2004.12.004

Familial Parry-Romberg disease

Peter J. Anderson^*, Darren Molony, Eric Haan, David J. David

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

29 Citations (Scopus)

Abstract

Parry-Romberg disease (or hemifacial atrophy) is a rare condition affecting the face. It commences in childhood but its aetiology remains unknown, and is sporadic. Two cases are presented who were biological first cousins. We believe that this is the first recorded example of this condition occurring in family members.

Original language	English
Pages (from-to)	705-708
Number of pages	4
Journal	International Journal of Pediatric Otorhinolaryngology
Volume	69
Issue number	5
DOIs	https://doi.org/10.1016/j.ijporl.2004.12.004
Publication status	Published - May 2005
Externally published	Yes

Keywords

Face
Hemifacial atrophy
Parry-Romberg disease

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10.1016/j.ijporl.2004.12.004

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title = "Familial Parry-Romberg disease",

abstract = "Parry-Romberg disease (or hemifacial atrophy) is a rare condition affecting the face. It commences in childhood but its aetiology remains unknown, and is sporadic. Two cases are presented who were biological first cousins. We believe that this is the first recorded example of this condition occurring in family members.",

keywords = "Face, Hemifacial atrophy, Parry-Romberg disease",

author = "Anderson, {Peter J.} and Darren Molony and Eric Haan and David, {David J.}",

year = "2005",

month = may,

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language = "English",

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T1 - Familial Parry-Romberg disease

AU - Anderson, Peter J.

AU - Molony, Darren

AU - Haan, Eric

AU - David, David J.

PY - 2005/5

Y1 - 2005/5

N2 - Parry-Romberg disease (or hemifacial atrophy) is a rare condition affecting the face. It commences in childhood but its aetiology remains unknown, and is sporadic. Two cases are presented who were biological first cousins. We believe that this is the first recorded example of this condition occurring in family members.

AB - Parry-Romberg disease (or hemifacial atrophy) is a rare condition affecting the face. It commences in childhood but its aetiology remains unknown, and is sporadic. Two cases are presented who were biological first cousins. We believe that this is the first recorded example of this condition occurring in family members.

KW - Face

KW - Hemifacial atrophy

KW - Parry-Romberg disease

UR - http://www.scopus.com/inward/record.url?scp=17844389827&partnerID=8YFLogxK

U2 - 10.1016/j.ijporl.2004.12.004

DO - 10.1016/j.ijporl.2004.12.004

M3 - Article

C2 - 15850693

AN - SCOPUS:17844389827

SN - 0165-5876

VL - 69

SP - 705

EP - 708

JO - International Journal of Pediatric Otorhinolaryngology

JF - International Journal of Pediatric Otorhinolaryngology

IS - 5

ER -

Familial Parry-Romberg disease

Abstract

Keywords

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