Optic nerve findings in CHILD syndrome.

Robert M. Knape; Kunjal B. Gandhi; Sanjeev Y. Tuli; Nausheen Khuddus

doi:10.3928/01913913-20100920-06

Optic nerve findings in CHILD syndrome.

Robert M. Knape
, Kunjal B. Gandhi
, Sanjeev Y. Tuli
, Nausheen Khuddus

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

6 Scopus citations

Abstract

Congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome is a rare disorder characterized by birth defects of several organ systems, including the skin, viscera, musculoskeletal system, and central nervous system. The authors present the first report of CHILD syndrome with ocular manifestations in a patient with progressive bilateral optic nerve atrophy.

Original language	English (US)
Pages (from-to)	e1-3
Journal	Journal of Pediatric Ophthalmology and Strabismus
Volume	47 Online
DOIs	https://doi.org/10.3928/01913913-20100920-06
State	Published - 2010
Externally published	Yes

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Ophthalmology

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10.3928/01913913-20100920-06

Cite this

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title = "Optic nerve findings in CHILD syndrome.",

abstract = "Congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome is a rare disorder characterized by birth defects of several organ systems, including the skin, viscera, musculoskeletal system, and central nervous system. The authors present the first report of CHILD syndrome with ocular manifestations in a patient with progressive bilateral optic nerve atrophy.",

author = "Knape, \{Robert M.\} and Gandhi, \{Kunjal B.\} and Tuli, \{Sanjeev Y.\} and Nausheen Khuddus",

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doi = "10.3928/01913913-20100920-06",

language = "English (US)",

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T1 - Optic nerve findings in CHILD syndrome.

AU - Knape, Robert M.

AU - Gandhi, Kunjal B.

AU - Tuli, Sanjeev Y.

AU - Khuddus, Nausheen

PY - 2010

Y1 - 2010

N2 - Congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome is a rare disorder characterized by birth defects of several organ systems, including the skin, viscera, musculoskeletal system, and central nervous system. The authors present the first report of CHILD syndrome with ocular manifestations in a patient with progressive bilateral optic nerve atrophy.

AB - Congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome is a rare disorder characterized by birth defects of several organ systems, including the skin, viscera, musculoskeletal system, and central nervous system. The authors present the first report of CHILD syndrome with ocular manifestations in a patient with progressive bilateral optic nerve atrophy.

UR - https://www.scopus.com/pages/publications/84891759434

UR - https://www.scopus.com/pages/publications/84891759434#tab=citedBy

U2 - 10.3928/01913913-20100920-06

DO - 10.3928/01913913-20100920-06

M3 - Article

C2 - 20886807

AN - SCOPUS:84891759434

SN - 0191-3913

VL - 47 Online

SP - e1-3

JO - Journal of Pediatric Ophthalmology and Strabismus

JF - Journal of Pediatric Ophthalmology and Strabismus

ER -

Optic nerve findings in CHILD syndrome.

Abstract

ASJC Scopus subject areas

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