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
(59.0%)
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.
Micrognathia Short nose
Child, Preschool Chromosome Aberrations Chromosome Deletion Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 2 Homo sapiens Infant Infant, Newborn Intellectual Disability Male Trisomy
2
(57.8%)
3056149
[Complete triploidy in a live newborn infant. Review and contribution of a new case].
Gillem Lanuza F, Vargas Torcal F, Amelin Chauve MC, Gabarra Lamas J.
An Esp Pediatr. 1988;29(2):143-8.
Micrognathia
Homo sapiens Infant, Newborn Male Polyploidy
3
(40.9%)
7844681
Congenital cytomegalovirus infection as a result of nonprimary cytomegalovirus disease in a mother with acquired immunodeficiency syndrome.
Schwebke K, Henry K, Balfour HH Jr, Olson D, Crane RT, Jordan MC.
J Pediatr. 1995;126(2):293-5.
Sinusitis
AIDS-Related Opportunistic Infections Adult Cytomegalovirus Infections Fatal Outcome Females Fetal Diseases Homo sapiens Hyaline Membrane Disease Infant, Newborn Lung Diseases, Interstitial Male Pregnancy Pregnancy Complications, Infectious Preterm Infant Viremia
4
(39.0%)
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.
Mild microcephaly
Beckwith-Wiedemann Syndrome General Anesthesia Homo sapiens Infant, Newborn Infant, Premature, Diseases Male
5
(34.6%)
2414108
Neonatal nemaline myopathy presenting with multiple joint contractures.
Bucher HU, Boltshauser E, Briner J.
Eur J Pediatr. 1985;144(3):288-90.
Cryptorchidism Hip dislocation Absent palmar crease
Arthrogryposis Electron Microscopy Homo sapiens Inclusion Bodies Infant, Newborn Male Muscle Tissue Myopathy Staining and Labeling
6
(29.4%)
3831902
[Branhamella catarrhalis in neonatal pulmonary infectious pathology].
Haddad J, Lefaou A, Simeoni U, Messer J.
Pediatrie. 1985;40(7):553-6.
Conjunctivitis
Bacterial Infections Females Homo sapiens Hyaline Membrane Disease Infant, Newborn Male Neisseriaceae Pneumonia Preterm Infant Trachea
7
(17.5%)
7206762
Extracorporeal membrane oxygenation. Successful treatment of persistent fetal circulation following repair of congenital diaphragmatic hernia.
Hardesty RL, Griffith BP, Debski RF, Jeffries MR, Borovetz HS.
J Thorac Cardiovasc Surg. 1981;81(4):556-63.
Hypertension Hernia
Blood Flow Velocity Blood Gas Analysis Diaphragmatic Hernia Females Heart-Lung Machine Homo sapiens Hypoxia Infant, Newborn Male Oxygenators, Membrane Persistent Fetal Circulation Syndrome Respiratory Distress Syndrome, Newborn Vasodilator Agents Whole Blood Coagulation Time
7
(17.5%)
2545215
Infantile cytochrome c oxidase deficiency with neonatal death.
Takayanagi T, Inoue M, Tomimasu K, Shimomura C, Matsuzaka T, Tsuji Y, Nonaka I.
Pediatr Neurol. 1989;5(3):179-81.
Respiratory insufficiency Generalized muscle weakness
Cytochrome-c Oxidase Deficiency Homo sapiens Infant, Newborn Male
7
(17.5%)
442315
Intrathoracic kidney.
Ramos AJ, Slovis TL, Reed JO.
Urology. 1979;13(1):14-9.
Respiratory tract infection Hernia
Chest Child, Preschool Females Homo sapiens Infant Infant, Newborn Kidney Male Preterm Infant Radiography, Thoracic
10
(4.0%)
31039513
Case report of a laryngotracheal reconstruction with anterior and posterior costal cartilage graft and stent placement - Surgical technique.
Albrecht NM, Ostrower S.
Int J Surg Case Rep. 2019;58:145-152.
Laryngomalacia
        

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