Neonatal lupus erythematosus




Input patient's signs and symptoms


Narrow down the case reports



Total: 104 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
97
(5.0%)
12664034
Persistent scarring, atrophy, and dyspigmentation in a preteen girl with neonatal lupus erythematosus.
High WA, Costner MI.
J Am Acad Dermatol. 2003;48(4):626-8.
Scarring
Child Cicatrix Facial Dermatoses Females Homo sapiens Hyperpigmentation Infant, Newborn Lupus Erythematosus, Cutaneous Skin
97
(5.0%)
12558850
Central nervous system involvement in neonatal lupus erythematosus.
Prendiville JS, Cabral DA, Poskitt KJ, Au S, Sargent MA.
Pediatr Dermatol. 2003;20(1):60-7.
Macrocephaly
Adult Cerebral Ventriculography Females Follow-Up Studies Health Risk Assessment Homo sapiens Infant, Newborn Lupus Erythematosus, Systemic Lupus Vasculitis, Central Nervous System Male Pregnancy Pregnancy Complications Severity of Illness Index Ultrasonography, Prenatal
97
(5.0%)
12053545
[Neonatal lupus erythematosus and neurologic involvement: an incidental association?].
Besson-Leaud L, Fontan D, Billeaud C, Sandler B.
Arch Pediatr. 2002;9(5):503-5.
Spastic paraparesis
SNRNP70 SSB
Antibodies, Anticardiolipin Antibodies, Antinuclear Females Homo sapiens Infant Lupus Erythematosus, Systemic Paraparesis, Spastic
97
(5.0%)
12043891
Ultraviolet light exposure is not a requirement for the development of cutaneous neonatal lupus.
Cimaz R, Biggioggero M, Catelli L, Muratori S, Cambiaghi S.
Lupus. 2002;11(4):257-60.
Scarring
SSB
Adult Females Homo sapiens Infant, Newborn Lupus Erythematosus, Cutaneous Pregnancy Ultraviolet Rays
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 33

HPO ID Term # of case reports
HP:0012115 Hepatitis 6
HP:0012722 Heart block 6
HP:0010783 Erythema 4
HP:0001678 Atrioventricular block 3
HP:0001873 Thrombocytopenia 3
HP:0001903 Anemia 2
HP:0100699 Scarring 2
HP:0000822 Hypertension 1
HP:0000952 Jaundice 1
HP:0000979 Purpura 1
HP:0001009 Telangiectasia 1
HP:0001041 Facial erythema 1
HP:0001045 Vitiligo 1
HP:0001056 Milia 1
HP:0001250 Seizures 1
HP:0001369 Arthritis 1
HP:0001395 Hepatic fibrosis 1
HP:0001433 Hepatosplenomegaly 1
HP:0001662 Bradycardia 1
HP:0001744 Splenomegaly 1
HP:0001876 Pancytopenia 1
HP:0001945 Fever 1
HP:0002196 Myelopathy 1
HP:0002313 Spastic paraparesis 1
HP:0002960 Autoimmunity 1
HP:0012733 Macule 1
HP:0012819 Myocarditis 1
HP:0025085 Bloody diarrhea 1
HP:0025104 Capillary malformation 1
HP:0025528 Annular cutaneous lesion 1
HP:0030350 Erythematous papule 1
HP:0200034 Papule 1
HP:0410266 Visceral hemangioma 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID