Ptosis, and Postaxial hand polydactyly

Diseases related with Ptosis and Postaxial hand polydactyly

In the following list you will find some of the most common rare diseases related to Ptosis and Postaxial hand polydactyly that can help you solving undiagnosed cases.


Top matches:

Medium match JOUBERT SYNDROME 7; JBTS7


Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Generalized hypotonia
  • Scoliosis
  • Ataxia


SOURCES: OMIM MESH MENDELIAN

More info about JOUBERT SYNDROME 7; JBTS7

Medium match MEGALENCEPHALY-POLYMICROGYRIA-POSTAXIAL POLYDACTYLY-HYDROCEPHALUS SYNDROME


Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome is characterized by megalencephaly, polymicrogyria, and hydrocephalus with variable polydactyly. It has been described in six unrelated patients. Intellectual deficit or slow development is also present. The mode of inheritance of this syndrome is unknown since all cases were sporadic.

MEGALENCEPHALY-POLYMICROGYRIA-POSTAXIAL POLYDACTYLY-HYDROCEPHALUS SYNDROME Is also known as meg-pmg-megacc syndrome|mpph syndrome|megalencephaly, polymicrogyria, mega corpus callosum syndrome|mpph|megalencephaly, mega corpus callosum, and complete lack of motor development

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hypertelorism


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about MEGALENCEPHALY-POLYMICROGYRIA-POSTAXIAL POLYDACTYLY-HYDROCEPHALUS SYNDROME

Medium match JOUBERT SYNDROME 1; JBTS1


Joubert syndrome is a clinically and genetically heterogeneous group of disorders characterized by hypoplasia of the cerebellar vermis with the characteristic neuroradiologic 'molar tooth sign,' and accompanying neurologic symptoms, including dysregulation of breathing pattern and developmental delay. Other variable features include retinal dystrophy and renal anomalies (Saraiva and Baraitser, 1992; Valente et al., 2005). Genetic Heterogeneity of Joubert SyndromeSee also JBTS2 (OMIM ), caused by mutation in the TMEM216 gene (OMIM ) on chromosome 11q13; JBTS3 (OMIM ), caused by mutation in the AHI1 gene (OMIM ) on chromosome 6q23; JBTS4 (OMIM ), caused by mutation in the NPHP1 gene (OMIM ) on chromosome 2q13; JBTS5 (OMIM ), caused by mutation in the CEP290 gene, also called NPHP6 (OMIM ), on chromosome 12q21.32; JBTS6 (OMIM ), caused by mutation in the TMEM67 gene (OMIM ) on chromosome 8q21; JBTS7 (OMIM ), caused by mutation in the RPGRIP1L gene (OMIM ) on chromosome 16q12.2; JBTS8 (OMIM ), caused by mutation in the ARL13B (OMIM ) on chromosome 3q11.2; JBTS9 (OMIM ), caused by mutation in the CC2D2A gene (OMIM ) on chromosome 4p15.3; JBTS10 (OMIM ), caused by mutation in the CXORF5 gene (OMIM ) on chromosome Xp22.3; JBTS11 (see {613820}), caused by mutation in the TTC21B gene (OMIM ) on chromosome 2q24; JBTS12 (see {200990}), caused by mutation in the KIF7 gene (OMIM ) on chromosome 15q26; JBTS13 (OMIM ), caused by mutation in the TCTN1 gene (OMIM ) on chromosome 12q24; JBTS14 (OMIM ), caused by mutation in the TMEM237 gene (OMIM ) on chromosome 2q33; JBTS15 (OMIM ), caused by mutation in the CEP41 gene (OMIM ) on chromosome 7q32; JBTS16 (OMIM ), caused by mutation in the TMEM138 gene (OMIM ) on chromosome 11q; JBTS17 (OMIM ), caused by mutation in the C5ORF42 gene (OMIM ) on chromosome 5p13; JBTS18 (OMIM ), caused by mutation in the TCTN3 gene (OMIM ) on chromosome 10q24; JBTS19 (see {614844}), caused by mutation in the ZNF423 gene (OMIM ) on chromosome 16q12; JBTS20 (OMIM ), caused by mutation in the TMEM231 gene (OMIM ) on chromosome 16q23; JBTS21 (OMIM ), caused by mutation in the CSPP1 gene (OMIM ) on chromosome 8q13; JBTS22 (OMIM ), caused by mutation in the PDE6D gene (OMIM ) on chromosome 2q37; JBTS23 (OMIM ), caused by mutation in the KIAA0586 gene (OMIM ) on chromosome 14q23; JBTS24 (OMIM ), caused by mutation in the TCTN2 gene (OMIM ) on chromosome 12q24; JBTS25 (OMIM ), caused by mutation in the CEP104 gene (OMIM ) on chromosome 1p36; JBTS26 (OMIM ), caused by mutation in the KIAA0556 gene (OMIM ) on chromosome 16p12; JBTS27 (OMIM ), caused by mutation in the B9D1 gene (OMIM ) on chromosome 17p11; JBTS28 (OMIM ), caused by mutation in the MKS1 gene (OMIM ) on chromosome 17q23; JBTS29 (see {617562}), caused by mutation in the TMEM107 gene (OMIM ) on chromosome 17p13; JBTS30 (OMIM ), caused by mutation in the ARMC9 gene (OMIM ) on chromosome 2q37; JBTS31 (OMIM ), caused by mutation in the CEP120 gene (OMIM ) on chromosome 5q23; JBTS32 (OMIM ), caused by mutation in the SUFU gene (OMIM ) on chromosome 10q24; and JBTS33 (OMIM ), caused by mutation in the PIBF1 gene (OMIM ) on chromosome 13q21.

JOUBERT SYNDROME 1; JBTS1 Is also known as cerebelloparenchymal disorder iv|jbts|cpd4|joubert syndrome|cerebellooculorenal syndrome 1|cors1|joubert-boltshauser syndrome

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Generalized hypotonia
  • Ataxia
  • Micrognathia


SOURCES: OMIM MENDELIAN

More info about JOUBERT SYNDROME 1; JBTS1

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Other less relevant matches:

Medium match JOUBERT SYNDROME WITH OCULORENAL DEFECT


Joubert syndrome with oculorenal defect is a rare subtype of Joubert syndrome and related disorders (JSRD, see this term) characterized by the neurological features of JS associated with both renal and ocular disease.

JOUBERT SYNDROME WITH OCULORENAL DEFECT Is also known as coloboma, chorioretinal, with cerebellar vermis aplasia|arima syndrome|js-or|js type b|cerebellooculorenal syndrome|joubert syndrome with senior-loken syndrome|cors|joubert syndrome with bilateral chorioretinal coloboma|cerebrooculohepatorenal syndrome|de

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Scoliosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about JOUBERT SYNDROME WITH OCULORENAL DEFECT

Medium match LATHOSTEROLOSIS


Lathosterolosis is an extremely rare inborn error of sterol biosynthesis characterized by facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease.

LATHOSTEROLOSIS Is also known as sc5d deficiency|sterol c5-desaturase deficiency

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about LATHOSTEROLOSIS

Medium match ULNAR-MAMMARY SYNDROME


Ulnar-mammary syndrome (UMS) is a rare developmental disorder characterized by ulnar defects, mammary and apocrine gland hypoplasia and genital anomalies. Delayed puberty dental anomalies, short stature and obesity have also been described.

ULNAR-MAMMARY SYNDROME Is also known as schinzel syndrome|ums|pallister ulnar-mammary syndrome

Related symptoms:

  • Short stature
  • Growth delay
  • Hypertelorism
  • Cryptorchidism
  • Ptosis


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about ULNAR-MAMMARY SYNDROME

Medium match JOUBERT SYNDROME WITH HEPATIC DEFECT


Joubert syndrome with hepatic defect is a very rare subtype of Joubert syndrome and related disorders (JSRD, see this term) characterized by the neurological features of JS associated with congenital hepatic fibrosis (CHF).

JOUBERT SYNDROME WITH HEPATIC DEFECT Is also known as coach syndrome|cerebellar vermis hypoplasia-oligophrenia-congenital ataxia-coloboma-hepatic fibrosis|cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, ocular coloboma, and hepatic fibrosis|js-h|joubert syndrome with congenital hepatic fibro

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Scoliosis


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about JOUBERT SYNDROME WITH HEPATIC DEFECT

Medium match LOEYS-DIETZ SYNDROME 1; LDS1


The Loeys-Dietz syndrome (LDS) is an autosomal dominant aortic aneurysm syndrome with widespread systemic involvement. As defined by Loeys et al. (2006), the disorder is characterized by the triad of arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate. Some patients have craniofacial involvement consisting of cleft palate, craniosynostosis, or hypertelorism. Bifid uvula may also be present. The natural history is characterized by aggressive arterial aneurysms and a high rate of pregnancy-related complications.LDS is also associated with immunologic-related disorders: approximately one-third of affected individuals exhibit food allergies, in contrast to a prevalence of 6 to 8% in the general population, and LDS patients have an increased prevalence of asthma, rhinitis, and eczema (summary by MacCarrick et al., 2014). NomenclatureIn initial reports, LDS patients, defined as those with mutations in TGFBR1 or TGFBR2, were stratified into 2 types, depending on severity of craniofacial features (type 1) or cutaneous features (type 2) (MacCarrick et al., 2014). Given that vascular disease is the major concern in LDS irrespective of the severity of systemic features, a revised nosology was proposed with sequential numbering corresponding to the gene mutant in each group (see below). Genetic Heterogeneity of Loeys-Dietz SyndromeLDS1 is caused by mutation in the TGFBR1 gene. LDS2 (OMIM ) is caused by mutation in the TGFBR2 gene (OMIM ). LDS3 (OMIM ), which is associated with early-onset osteoarthritis, is caused by mutation in the SMAD3 gene (OMIM ). LDS4 (OMIM ) is caused by mutation in the TGFB2 gene (OMIM ). LDS5 (OMIM ) is caused by mutation in the TGFB3 gene (OMIM ). ReviewsMacCarrick et al. (2014) provided a review of LDS, stating that there are no specific clinical criteria for the diagnosis, which is confirmed by molecular testing. They proposed that mutation in any of the 4 genes, TGFBR1, TGFBR2, SMAD3, or TGFB2, in combination with arterial aneurysm or dissection or a family history of documented LDS, should be sufficient to establish the diagnosis. The authors noted that rapidly progressive aortic aneurysmal disease is a distinct feature of LDS, and they discussed management strategies for cardiovascular issues as well as other complications of LDS.

LOEYS-DIETZ SYNDROME 1; LDS1 Is also known as aat5|aortic aneurysm, familial thoracic 5|loeys-dietz aortic aneurysm syndrome|furlong syndrome

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Scoliosis
  • Hypertelorism
  • Micrognathia


SOURCES: OMIM MENDELIAN

More info about LOEYS-DIETZ SYNDROME 1; LDS1

Medium match PALLISTER-HALL SYNDROME; PHS


Pallister-Hall syndrome is a pleiotropic autosomal dominant disorder comprising hypothalamic hamartoma, pituitary dysfunction, central polydactyly, and visceral malformations (Biesecker et al., 1996).

PALLISTER-HALL SYNDROME; PHS Is also known as hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Growth delay


SOURCES: OMIM MESH MENDELIAN

More info about PALLISTER-HALL SYNDROME; PHS

Medium match CEREBROFACIOTHORACIC DYSPLASIA


Cerebro-facio-thoracic dysplasia or Pascual-Castroviejo syndrome type 1 is a rare syndrome characterized by facial dysmorphism, intellectual deficit and costovertebral abnormalities.

CEREBROFACIOTHORACIC DYSPLASIA Is also known as pascual-castroviejo syndrome type 1|cerebrofaciothoracic dysplasia

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Microcephaly


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about CEREBROFACIOTHORACIC DYSPLASIA

Top 5 symptoms//phenotypes associated to Ptosis and Postaxial hand polydactyly

Symptoms // Phenotype % cases
Intellectual disability Very Common - Between 80% and 100% cases
Global developmental delay Very Common - Between 80% and 100% cases
Generalized hypotonia Common - Between 50% and 80% cases
Growth delay Common - Between 50% and 80% cases
Polydactyly Common - Between 50% and 80% cases
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Other less frequent symptoms

Patients with Ptosis and Postaxial hand polydactyly. may also develop some of the following symptoms:

Common Symptoms - More than 50% cases


Anteverted nares

Uncommon Symptoms - Between 30% and 50% cases


Micrognathia Macrocephaly Hypertelorism Seizures Renal cyst Postaxial polydactyly Downslanted palpebral fissures Abnormality of the kidney Scoliosis Muscular hypotonia Apnea Strabismus Inguinal hernia Retinal dystrophy Hernia Ataxia Talipes equinovarus Encephalocele Hydrocephalus Cerebellar vermis hypoplasia Abnormal facial shape Molar tooth sign on MRI Highly arched eyebrow Chorioretinal coloboma Absent speech Epicanthus Pectus carinatum Growth hormone deficiency Intellectual disability, severe Biparietal narrowing Short stature Hepatomegaly Hepatic fibrosis Postaxial foot polydactyly Cryptorchidism Narrow forehead Long face Prominent nasal bridge Coloboma High palate Mandibular prognathia Low-set ears Short nose Atrial septal defect Visual impairment Hypoplasia of the corpus callosum Occipital encephalocele Nystagmus Renal insufficiency Abnormality of the eye Abnormality of eye movement Stage 5 chronic kidney disease Apraxia Renal hypoplasia Cleft palate Oculomotor apraxia Hypoplasia of the brainstem Nephronophthisis Patent ductus arteriosus Tremor Abnormality of the liver Brainstem dysplasia Ventricular septal defect Frontal bossing Wide mouth Posteriorly rotated ears

Rare Symptoms - Less than 30% cases


Hypertension Aplasia/Hypoplasia of the corpus callosum Abnormality of neuronal migration Abnormality of cardiovascular system morphology Multicystic kidney dysplasia Nephropathy Abnormality of the hypothalamus-pituitary axis Iris coloboma Dyspnea Rib fusion Microcephaly Multiple small medullary renal cysts Low-set, posteriorly rotated ears Hand polydactyly Oral cleft Hepatosplenomegaly Aplasia/Hypoplasia of the cerebellar vermis Camptodactyly Wide nasal bridge Micropenis Dilatation Hypospadias Pes planus Craniosynostosis Bifid uvula Microretrognathia Sprengel anomaly Shawl scrotum Oligodactyly External genital hypoplasia Abnormality of the genital system Round face Wide nose Anal atresia Upslanted palpebral fissure Intrauterine growth retardation Cholestasis Syndactyly Elevated hepatic transaminase Toe syndactyly Talipes Thin vermilion border Hypoplasia of penis Gingival overgrowth Feeding difficulties Arnold-Chiari malformation Portal hypertension Hemivertebrae Renal agenesis Cleft upper lip Hydronephrosis Behavioral abnormality Congenital hepatic fibrosis Neonatal breathing dysregulation Ventriculomegaly Self-mutilation Tachypnea Prominent forehead Large for gestational age Motor delay Optic nerve coloboma Depressed nasal bridge Cerebellar hypoplasia Agenesis of cerebellar vermis Blindness Abnormal pattern of respiration Heterotopia Pachygyria Telecanthus Downturned corners of mouth Episodic tachypnea Mitral regurgitation Central apnea Meningoencephalocele Narrow nose High anterior hairline Dilatation of the cerebral artery Soft skin Scaphocephaly Sagittal craniosynostosis Rhinitis Aortic root aneurysm Abnormality of the sternum Conical tooth Atrophic scars Disproportionate tall stature Spondylolisthesis Short neck Rectovaginal fistula Beaking of vertebral bodies Descending thoracic aorta aneurysm Pulmonary artery aneurysm Neurodevelopmental delay Vertebral segmentation defect Multiple suture craniosynostosis Vertebral fusion Cystic medial necrosis Ascending aortic dissection Long toe Long thorax Dural ectasia Abnormal hair pattern Unilateral ptosis Arterial tortuosity Hallux valgus Ascending tubular aorta aneurysm Dermal translucency Thoracic aortic aneurysm Finger clinodactyly Myopathic facies Intrahepatic biliary atresia Clinodactyly of the 5th finger Bull's eye maculopathy Clinodactyly Poliosis Malar flattening Abnormality of the skeletal system Myopia Exodeviation Chronic hepatic failure Proptosis Cholestatic liver disease Esophageal varix Neoplasm of the liver Abnormality of abdomen morphology Aplasia/Hypoplasia of the cerebellum Chronic kidney disease Bifid ribs Gastrointestinal hemorrhage Intestinal malrotation Hyperextensibility of the finger joints Kyphoscoliosis Aortic aneurysm Mitral valve prolapse Ectopia lentis Bicuspid aortic valve Joint dislocation Bicuspid pulmonary valve Joint contracture of the hand Exotropia Osteoarthritis Blue sclerae Eczema Retrognathia Asthma Bruising susceptibility Arachnodactyly Facial asymmetry Dolichocephaly Broad forehead Broad philtrum Joint laxity Skeletal dysplasia Generalized arterial tortuosity Microphthalmia Supernumerary nipple Microphallus Radial head subluxation Postnatal growth retardation Attention deficit hyperactivity disorder Hydrometrocolpos Hypoplasia of the epiglottis Narrow chest Mandibular aplasia Bilateral choanal atresia Vaginal atresia Hypothalamic hamartoma Synophrys Unsteady gait Panhypopituitarism Joint hypermobility Flat face Thick eyebrow Hypoplasia of the maxilla Vesicoureteral reflux Decreased circulating cortisol level Laryngeal cleft Mesoaxial polydactyly Upper airway obstruction Distal shortening of limbs Mesoaxial foot polydactyly Midface retrusion Pectus excavatum Hyporeflexia Brachycephaly Cerebral cortical atrophy Hypothyroidism Midline facial capillary hemangioma Polyhydramnios Thyroid dysgenesis Preductal coarctation of the aorta Primitive neuroectodermal tumor Neonatal hypotonia Bifid epiglottis Anxiety Distal urethral duplication Y-shaped metacarpals Mesoaxial hand polydactyly Cleft lip Wide intermamillary distance Short 4th metacarpal Overlapping toe Single transverse palmar crease Holoprosencephaly Sacral dimple Renal dysplasia Choanal atresia Small nail Limb undergrowth Decreased testicular size Nail dysplasia Coarse hair Sparse eyelashes Hip dislocation Microtia Respiratory tract infection Respiratory failure Abnormal heart morphology Diverticulosis of trachea Brachydactyly Neoplasm Biconvex vertebral bodies Cutaneous syndactyly Scrotal hypoplasia Microglossia Natal tooth Adrenal hypoplasia Decreased fetal movement Abnormal lung lobation Abnormality of the ribs Low posterior hairline Intention tremor Hypopituitarism Hamartoma Mesomelia Low anterior hairline Hydroureter Ectopic kidney Adrenal insufficiency Long eyelashes Tall stature Sparse and thin eyebrow Bilateral cryptorchidism Precocious puberty Atresia of the external auditory canal Cirrhosis Laryngomalacia Feeding difficulties in infancy Polyuria Renal corticomedullary cysts Tubulointerstitial fibrosis Dilated fourth ventricle Undetectable electroretinogram Tubular atrophy Foot polydactyly Severe vision loss Congenital blindness Polydipsia Renal sodium wasting Polycystic kidney dysplasia Intellectual disability, progressive Aganglionic megacolon Hepatic steatosis Severe global developmental delay Autistic behavior Anemia Triangular-shaped open mouth Occipital myelomeningocele Occipital meningocele Hearing impairment Enlarged fossa interpeduncularis Full cheeks Pathologic fracture Bilateral talipes equinovarus Elevated alkaline phosphatase Opacification of the corneal stroma Hyperbilirubinemia Horseshoe kidney Sloping forehead Cerebral calcification Specific learning disability Microcornea Failure to thrive Bulbous nose Hepatic failure Conductive hearing impairment Osteoporosis Myoclonus Thrombocytopenia Cerebral atrophy Long philtrum Cataract Hemifacial spasm Dysgenesis of the cerebellar vermis Meningocele High forehead Long palpebral fissure Infantile spasms Cortical dysplasia Knee flexion contracture Intellectual disability, profound Polymicrogyria Abnormal cardiac septum morphology Muscular hypotonia of the trunk Narrow mouth Megalencephaly Kyphosis Skeletal muscle atrophy Absence of renal corticomedullary differentiation Abnormal corpus callosum morphology Severe postnatal growth retardation Abnormal retinal morphology Mutism Horizontal nystagmus Genu valgum Thoracic scoliosis Abnormally large globe Elongated superior cerebellar peduncle Abnormality of skin pigmentation Abnormality of ocular smooth pursuit Abnormal saccadic eye movements Breathing dysregulation Impaired smooth pursuit Retinal dysplasia Protruding tongue Open mouth Dandy-Walker malformation Macroglossia Abnormality of the foot Dilation of lateral ventricles Aggressive behavior Hyperactivity Cognitive impairment Thick corpus callosum Vascular ring Capillary malformation Abnormal nasal morphology Cavum septum pellucidum Abnormal localization of kidney Prominent metopic ridge Myelomeningocele Intellectual disability, moderate Wide nasal base Laryngeal stenosis Aplasia/Hypoplasia of the ulna Broad eyebrow Subglottic stenosis Gastroschisis Breast aplasia Anterior pituitary hypoplasia Abnormality of the humerus Breast hypoplasia Abnormality of the radius Perimembranous ventricular septal defect Gonadotropin deficiency Broad face Abnormality of the uterus Wolff-Parkinson-White syndrome Sparse lateral eyebrow Sparse axillary hair Supraventricular tachycardia Ectopic anus Abnormality of temperature regulation Absent hand Hypoplastic scapulae Long uvula Abnormality of the nervous system Agenesis of corpus callosum Splenomegaly Gait disturbance Hyperreflexia Spasticity Unilateral oligodactyly Axillary apocrine gland hypoplasia Deformed radius Short 5th toe Ectopic posterior pituitary Short 4th toe Imperforate hymen Aplasia of the pectoralis major muscle Laryngeal web Hernia of the abdominal wall Absent axillary hair Abnormal external genitalia Body odor Aplasia of the ulna Abnormality of the wrist Abnormality of finger Intrahepatic cholestasis Abnormality of cholesterol metabolism Arrhythmia Obesity Abnormality of the dentition Abnormality of the thoracic spine Lumbosacral meningocele Bilobate gallbladder Foam cells with lamellar inclusion bodies Severe generalized osteoporosis Schistocytosis Abnormal platelet morphology Camptodactyly of finger Cerebellar cortical atrophy Anisopoikilocytosis Neural tube defect Increased mean platelet volume Butterfly vertebrae Ambiguous genitalia, male Generalized osteoporosis Acanthocytosis Thick upper lip vermilion Hyperhidrosis Delayed puberty Abnormality of the clavicle Hypoplastic toenails Short clavicles Inverted nipples Absent radius Anal stenosis Hypoplastic nipples Short humerus Hyperthyroidism Decreased fertility Hypoplasia of the ulna Bifid scrotum Tachycardia Pyloric stenosis Hypoplasia of the radius Abnormality of the metacarpal bones Abnormality of the fingernails Split hand Interphalangeal joint contracture of finger Convex nasal ridge Hypodontia Short distal phalanx of finger Microdontia of primary teeth



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