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)
1
(54.2%)
15181498
Neonatal lupus erythematosus with cholestatic hepatitis.
Lin SC, Shyur SD, Huang LH, Wu JY, Chuo HT, Lee HC.
J Microbiol Immunol Infect. 2004;37(2):131-4.
Jaundice Anemia Conjugated hyperbilirubinemia
SNRNP70 SSB TRIM21
Anemia Antibodies, Antinuclear Autoantibodies Autoantigens Cholestasis Hepatitis Homo sapiens Infant Infant, Newborn Lupus Erythematosus, Systemic Male Ribonucleoproteins Thrombocytopenia Transaminases
2
(53.5%)
18353232
[Neonatal lupus erythematosus: analysis of 8 cases].
Yang Q, Shao XM, Cao Y, Chen C, Cheng GQ, Shi YY, Zhou LJ.
Zhonghua Er Ke Za Zhi. 2008;46(1):18-21.
Cholestasis Hepatosplenomegaly Anemia
SSB TRIM21
Autoimmune Diseases Females Homo sapiens Infant Infant, Newborn Lupus Erythematosus, Cutaneous Male Retrospective Studies
3
(52.7%)
1845364
Neonatal lupus erythematosus with multisystem organ involvement preceding cutaneous lesions.
Fonseca E, Contreras F, Garcia-Frias E, Carrascosa MC.
Lupus. 1991;1(1):49-50.
Purpura Splenomegaly Anemia
Adult Autoantigens Females Homo sapiens Infant, Newborn Lupus Erythematosus, Systemic RNA, Small Cytoplasmic Ribonucleoproteins
4
(50.0%)
512088
Neonatal lupus erythematosus.
Draznin TH, Esterly NB, Furey NL, DeBofsky H.
J Am Acad Dermatol. 1979;1(5):437-42.
Splenomegaly Anemia
Females Homo sapiens Infant Lupus Erythematosus, Discoid Lupus Erythematosus, Systemic Pregnancy Pregnancy Complications Skin
5
(45.7%)
8838929
Neonatal lupus erythematosus.
Hetem MB, Takada MH, Llorach Velludo MA, Foss NT.
Int J Dermatol. 1996;35(1):42-4.
Edema Leukopenia Anemia Follicular hyperkeratosis
NPPA TNFRSF25
Antibodies, Antinuclear Females Homo sapiens Infant Infant, Newborn Lupus Erythematosus, Cutaneous
5
(45.7%)
8362807
Aplastic anemia in neonatal lupus erythematosus.
Wolach B, Choc L, Pomeranz A, Ben Ari Y, Douer D, Metzker A.
Am J Dis Child. 1993;147(9):941-4.
Hyperkeratosis Anemia Metabolic acidosis Sepsis
C1QA CD8A TRIM21
Aplastic Anemia Erythroid Precursor Cells Females Hematopoiesis Homo sapiens Immune Tolerance Infant Lupus Erythematosus, Discoid
7
(44.2%)
23839605
Neonatal lupus with atypical cardiac and cutaneous manifestation.
Morais S, Santos IC, Pereira DF, Mimoso G.
BMJ Case Rep. 2013;2013:.
Hepatosplenomegaly Thrombocytopenia Unexplained fevers
SSB
Aged, 80 and over Heart Diseases Homo sapiens Lupus Erythematosus, Systemic Male
8
(42.9%)
15624375
Facial telangiectasia-an unusual complication of neonatal lupus erythematosus: report of one case.
Lin SC, Shyur SD, Wu JY, Huang LH.
Acta Paediatr Taiwan. 2004;45(4):246-8.
Telangiectasia Hemolytic anemia
SNRNP70 SSB TRIM21
Antibodies, Antinuclear Differential Diagnosis Face Females Homo sapiens Infant Lupus Erythematosus, Cutaneous Telangiectasis
8
(42.9%)
10959907
Neonatal lupus erythematosus with microvascular hemolysis.
Hariharan D, Manno CS, Seri I.
J Pediatr Hematol Oncol. 2000;22(4):351-4.
Purpura Microangiopathic hemolytic anemia
Anemia, Hemolytic, Congenital Disseminated Intravascular Coagulation Females Glucocorticoids Homo sapiens Infant, Newborn Lupus Erythematosus, Systemic Plasma Platelet Transfusion Thrombocytopenia
10
(42.5%)
20523814
A case of neonatal lupus erythematosus showing transient anemia and hepatitis.
Kim KR, Yoon TY.
Ann Dermatol. 2009;21(3):315-8.
Anemia Hepatitis
SSB
        

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