Infant acute respiratory distress syndrome

Infant acute respiratory distress syndrome is a lung disorder that affects premature infants caused by developmental insufficiency of surfactant production and structural immaturity of the lungs. The symptoms usually appear shortly after birth and may include tachypnea, tachycardia, chest wall retractions (recession), expiratory grunting, nasal flaring and cyanosis during breathing efforts.



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Narrow down the case reports



Total: 116 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(49.7%)
16802574
[Severe respiratory distress due to ileal duplication cyst in the newborn].
Vukovic J, Sovagovic RG, Filipovic-Grcic B, Hlupic L, Jelasic D.
Acta Med Croatica. 2006;60(1):59-61.
Anemia Metabolic acidosis Abdominal mass
Atelectasis Differential Diagnosis Dyspnea Females Homo sapiens Infant, Newborn Infant, Premature, Diseases Respiratory Insufficiency
2
(32.8%)
1457118
Anesthetic considerations of an infant with Beckwith-Wiedemann syndrome.
Tobias JD, Lowe S, Holcomb GW 3rd.
J Clin Anesth. 1992;4(6):484-6.
Nevus flammeus Hypoglycemia Visceromegaly
Beckwith-Wiedemann Syndrome General Anesthesia Homo sapiens Infant, Newborn Infant, Premature, Diseases Male
3
(32.2%)
6879210
Unusual osteopathy in a newborn.
Jequier S, Nogrady MB, Wesenberg RL.
Skeletal Radiol. 1983;10(1):20-5.
Jaundice Hepatosplenomegaly
Homo sapiens Infant, Newborn Male Osteitis Osteomyelitis
4
(30.2%)
28542663
[Periorbital pallor post application of mydriatic in infants with hydrocephalus associated to systemic effects].
Alvarado Socarras JL, Rodriguez SC.
Rev Chil Pediatr. 2017;88(2):280-284.
Hydrocephalus Pallor Patent ductus arteriosus Intraventricular hemorrhage
Homo sapiens Hydrocephalus Infant, Newborn Low Birth Weight Infant Mydriatics Respiratory Distress Syndrome, Newborn
4
(30.2%)
3322008
A patient with partial duplication 2q and partial deficiency 11q.
Ho CK, Henderson KC, Bowyer FP, Eilers KB, Andrews LG.
Am J Med Genet. 1987;28(3):575-9.
Prominent occiput Abnormal dermatoglyphics Intraventricular hemorrhage
Child, Preschool Chromosome Aberrations Chromosome Deletion Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 2 Homo sapiens Infant Infant, Newborn Intellectual Disability Male Trisomy
6
(26.7%)
22120615
Surfactant therapy for maternal blood aspiration: an unusual cause of neonatal respiratory distress syndrome.
Celik IH, Demirel G, Canpolat FE, Erdeve O, Dilmen U.
Indian J Pediatr. 2012;79(10):1358-9.
Pneumonia Pulmonary hemorrhage Pulmonary edema
Abruptio Placentae Biological Products Females Homo sapiens Infant, Newborn Meconium Aspiration Syndrome Pregnancy Preterm Infant Pulmonary Surfactants Respiratory Distress Syndrome, Newborn
7
(25.0%)
1883179
High frequency oscillatory ventilation in neonates with respiratory distress.
Tan KL.
Ann Acad Med Singapore. 1991;20(2):219-22.
Cholestasis
Blood Gas Analysis Females High-Frequency Jet Ventilation Homo sapiens Hyaline Membrane Disease Infant, Newborn Male Survival Rate
7
(25.0%)
946401
Pulmonary yellow hyaline membrane disease. New variant in premature infants with intrahepatic cholestasis.
Cho SY, Sastre M.
Arch Pathol Lab Med. 1976;100(3):145-6.
Cholestasis
Cholestasis Cytoplasm Females Homo sapiens Hyaline Membrane Disease Infant, Newborn Liver Lung
9
(22.1%)
29910548
(5971647)
Clinicoetiological Pattern and Outcome of Neonates Requiring Mechanical Ventilation: Study in a Tertiary Care Centre.
Yadav M, Chauhan G, Bhardwaj AK, Sharma PD.
Indian J Crit Care Med. 2018;22(5):361-363.
Disseminated intravascular coagulation Intraventricular hemorrhage
9
(22.1%)
10410409
The anesthetic management of a preterm infant weighing 500 grams undergoing ligation of patent ductus arteriosus--a case report.
Chen KB, Tu KT, Cheng HC, Wu YL, Chang JS.
Acta Anaesthesiol Sin. 1999;37(2):89-92.
Patent ductus arteriosus Pulmonary hemorrhage
Adult Females Homo sapiens Infant, Newborn Intensive Care Units, Neonatal Ligation Pregnancy Preterm Infant
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 60

HPO ID Term # of case reports
HP:0002097 Emphysema 14
HP:0002098 Respiratory distress 9
HP:0002090 Pneumonia 7
HP:0002835 Aspiration 5
HP:0000822 Hypertension 3
HP:0001643 Patent ductus arteriosus 2
HP:0002789 Tachypnea 2
HP:0002878 Respiratory failure 2
HP:0004387 Enterocolitis 2
HP:0012418 Hypoxemia 2
HP:0030746 Intraventricular hemorrhage 2
HP:0031273 Shock 2
HP:0100750 Atelectasis 2
HP:0100806 Sepsis 2
HP:0000269 Prominent occiput 1
HP:0000347 Micrognathia 1
HP:0000369 Low-set ears 1
HP:0000737 Irritability 1
HP:0000796 Urethral obstruction 1
HP:0000821 Hypothyroidism 1
HP:0000952 Jaundice 1
HP:0000961 Cyanosis 1
HP:0001250 Seizures 1
HP:0001266 Choreoathetosis 1
HP:0001287 Meningitis 1
HP:0001321 Cerebellar hypoplasia 1
HP:0001433 Hepatosplenomegaly 1
HP:0001601 Laryngomalacia 1
HP:0001607 Subglottic stenosis 1
HP:0001635 Congestive heart failure 1
HP:0001662 Bradycardia 1
HP:0001695 Cardiac arrest 1
HP:0001873 Thrombocytopenia 1
HP:0001882 Leukopenia 1
HP:0001903 Anemia 1
HP:0001942 Metabolic acidosis 1
HP:0002045 Hypothermia 1
HP:0002093 Respiratory insufficiency 1
HP:0002094 Dyspnea 1
HP:0002107 Pneumothorax 1
HP:0002133 Status epilepticus 1
HP:0002170 Intracranial hemorrhage 1
HP:0002883 Hyperventilation 1
HP:0003196 Short nose 1
HP:0005521 Disseminated intravascular coagulation 1
HP:0006515 Interstitial pneumonitis 1
HP:0007477 Abnormal dermatoglyphics 1
HP:0010962 Extralobar sequestration 1
HP:0011726 Persistent fetal circulation 1
HP:0011947 Respiratory tract infection 1
HP:0011951 Aspiration pneumonia 1
HP:0012653 Status asthmaticus 1
HP:0025356 Psychomotor retardation 1
HP:0025421 Pneumomediastinum 1
HP:0030084 Clinodactyly 1
HP:0032445 Pulmonary cyst 1
HP:0040075 Hypopituitarism 1
HP:0040223 Pulmonary hemorrhage 1
HP:0100632 Pulmonary sequestration 1
HP:0200134 Epileptic encephalopathy 1


Causative gene(s) retrieved from Orphanet

    Total: 3

Gene Symbol Gene Name Entrez Gene ID
SFTPB surfactant protein B 6439
SFTPC surfactant protein C 6440
ABCA3 ATP binding cassette subfamily A member 3 21