105 studies found for:    "Craniofacial Abnormalities" OR "Baller-Gerold syndrome"
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Rank Status Study
21 Unknown  Genetic Modifiers for 22q11.2 Syndrome
Condition: 22q11.2 Deletion Syndrome
Intervention: Other: Observation
22 Completed Oral Cleft Prevention Trial in Brazil
Conditions: Cleft Lip;   Cleft Palate
Intervention: Drug: Folic acid (0.4mg vs. 4.0mg)
23 Completed Nautilus: Dynamic Craniotomy; New Surgical Technique and Preliminary Results
Condition: Children With Craniosynostoses
Intervention: Procedure: dynamic craniotomy
24 Withdrawn Comparison of Allogenix Plus Demineralized Bone Matrix and Autogenous Bone Dust Versus Autogenous Bone Dust Alone in Ossification of Small Calvarial Defects, a Pilot Study.
Condition: Metopic Craniosynostosis
Intervention: Biological: Allogenix Plus
25 Completed
Has Results
Simvastatin Therapy in Smith-Lemli-Opitz Syndrome
Condition: Smith-Lemli-Opitz Syndrome
Interventions: Drug: Simvastatin Susp.;   Drug: OraPlus
26 Completed
Has Results
Efficacy of Oral Versus Intravenous Acetaminophen for Primary Pediatric Cleft Palate Repair
Condition: Cleft Palate
Interventions: Drug: Oral acetaminophen;   Drug: Ofirmev®;   Drug: Opioid only
27 Active, not recruiting Thymus Transplantation With Immunosuppression
Conditions: DiGeorge Syndrome;   DiGeorge Anomaly;   Complete DiGeorge Anomaly;   Complete DiGeorge Syndrome
Intervention: Biological: Thymus Tissue for Transplantation
28 Unknown  Genetics and Psychopathology in the 22q11 Deletion Syndrome
Condition: Chromosome 22q11.2 Deletion Syndrome
Intervention:
29 Recruiting UAB HRFD Core Center: Core A: The Hepato/Renal Fibrocystic Diseases Translational Resource
Conditions: Hepato/Renal Fibrocystic Disease;   Autosomal Recessive Polycystic Kidney Disease;   Joubert Syndrome;   Bardet Biedl Syndrome;   Meckel-Gruber Syndrome;   Congenital Hepatic Fibrosis;   Caroli Syndrome;   Oro-Facial-Digital Syndrome Type I;   Nephronophthisis;   Glomerulocystic Kidney Disease
Intervention:
30 Completed Estimation of the Carrier Frequency and Incidence of Smith-Lemli-Opitz Syndrome in African Americans
Condition: Smith-Lemli-Opitz Syndrome
Intervention:
31 Completed Genetic Analysis of Craniosynostosis, Philadelphia Type
Conditions: Craniosynostosis;   Philadelphia Type Craniosynostosis
Intervention:
32 Not yet recruiting SNP-based Microdeletion and Aneuploidy RegisTry (SMART)
Conditions: 22q11 Deletion Syndrome;   DiGeorge Syndrome;   Trisomy 21;   Trisomy 18;   Trisomy 13;   Monosomy X;   Sex Chromosome Abnormalities;   Cri-du-Chat Syndrome;   Angelman Syndrome;   Prader-Willi Syndrome;   1p36 Deletion Syndrome
Intervention:
33 Recruiting The Efficacy and Population Pharmacokinetics of Tranexamic Acid for Craniosynostosis Surgery
Condition: Craniosynostosis
Interventions: Drug: high dose TXA;   Drug: Low dose TXA
34 Recruiting Genetic and Functional Analysis of Cherubism
Condition: Cherubism
Intervention:
35 Withdrawn Endoscopic Treatment for Isolated, Single Suture Craniosynostosis
Condition: Craniosynostosis
Intervention: Procedure: Endoscopic strip craniectomy
36 Unknown  Phase II Study of Dietary Cholesterol for Smith-Lemli-Opitz Syndrome
Condition: Smith-Lemli-Opitz Syndrome
Intervention: Behavioral: diet
37 Recruiting Qualitative and Quantitative Study Which Aims to Determine the Specifics of the Announcement for the Diagnosis of Patients With Craniosynostosis and Their Parents to Better Support Them in Their Care
Condition: Craniosynostosis
Interventions: Other: qualitative survey;   Other: quantitative survey
38 Terminated Infection in DiGeorge Following CHD Surgery
Conditions: DiGeorge Syndrome;   Congenital Heart Defects
Intervention:
39 Recruiting Microcephaly Genetic Deficiency in Neural Progenitors
Condition: Microcephaly
Intervention:
40 Recruiting Brain Characteristics Noted Prior to and Following Treatment
Condition: Nonsynostotic Plagiocephaly
Intervention: Other: Non-interventional

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Indicates status has not been verified in more than two years